Canonical Allele Identifier: CA771906448

Gene: GSDMB

Linked Data

• dbSNP Id: rs1484605292
• gnomAD v3: 17-39908054-G-T
• gnomAD v4: 17-39908054-G-T
• MyVariant Identifiers: chr17:g.38064307G>T (hg19) ; chr17:g.39908054G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39908054G>T , CM000679.2:g.39908054G>T	GRCh38
NC_000017.10:g.38064307G>T , CM000679.1:g.38064307G>T	GRCh37
NC_000017.9:g.35317833G>T	NCBI36
NG_015804.1:g.15597C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000418519.6:c.700+122C>A MANE Select	ENSP00000415049.1:n.700+122C>A
ENST00000309481.11:c.661+904C>A	ENSP00000312584.7:n.661+904C>A
ENST00000360317.7:c.700+122C>A	ENSP00000353465.3:n.700+122C>A
ENST00000394175.6:c.661+904C>A	ENSP00000377729.2:n.661+904C>A
ENST00000394179.5:c.661+904C>A	ENSP00000377733.2:n.661+904C>A
ENST00000418519.5:c.700+122C>A	ENSP00000415049.1:n.700+122C>A
ENST00000468820.1:c.187+1702C>A
ENST00000477054.6:n.3199+904C>A
ENST00000520542.5:c.700+122C>A	ENSP00000430157.1:n.700+122C>A
ENST00000522564.5:c.408-1067C>A	ENSP00000428217.1:n.408-1067C>A
ENST00000523371.5:c.577-1067C>A	ENSP00000429265.1:n.577-1067C>A
ENST00000524039.5:c.576+1702C>A	ENSP00000428712.1:n.576+1702C>A
NM_001042471.1:c.661+904C>A	NP_001035936.1:n.661+904C>A
NM_001165958.1:c.700+122C>A	NP_001159430.1:n.700+122C>A
NM_001165959.1:c.700+122C>A	NP_001159431.1:n.700+122C>A
NM_018530.2:c.661+904C>A	NP_061000.2:n.661+904C>A
XM_011525001.1:c.712+122C>A	XP_011523303.1:n.712+122C>A
XM_011525002.1:c.712+122C>A	XP_011523304.1:n.712+122C>A
XM_011525003.1:c.712+122C>A	XP_011523305.1:n.712+122C>A
XM_011525004.1:c.712+122C>A	XP_011523306.1:n.712+122C>A
XM_011525005.1:c.712+122C>A	XP_011523307.1:n.712+122C>A
XM_011525006.1:c.712+122C>A	XP_011523308.1:n.712+122C>A
XM_011525007.1:c.712+122C>A	XP_011523309.1:n.712+122C>A
XM_011525008.1:c.712+122C>A	XP_011523310.1:n.712+122C>A
XM_011525009.1:c.712+122C>A	XP_011523311.1:n.712+122C>A
XM_011525010.1:c.712+122C>A	XP_011523312.1:n.712+122C>A
XM_011525011.1:c.712+122C>A	XP_011523313.1:n.712+122C>A
XM_011525012.1:c.712+122C>A	XP_011523314.1:n.712+122C>A
XM_011525013.1:c.712+122C>A	XP_011523315.1:n.712+122C>A
XM_011525014.1:c.712+122C>A	XP_011523316.1:n.712+122C>A
XM_011525015.1:c.712+122C>A	XP_011523317.1:n.712+122C>A
XM_011525016.1:c.700+122C>A	XP_011523318.1:n.700+122C>A
XM_011525017.1:c.712+122C>A	XP_011523319.1:n.712+122C>A
XM_011525018.1:c.700+122C>A	XP_011523320.1:n.700+122C>A
XM_011525019.1:c.661+904C>A	XP_011523321.1:n.661+904C>A
XM_011525020.1:c.661+904C>A	XP_011523322.1:n.661+904C>A
XM_011525021.1:c.687+122C>A	XP_011523323.1:n.687+122C>A
XR_934504.1:n.2300+122C>A
NM_001369402.1:c.661+904C>A	NP_001356331.1:n.661+904C>A
NM_001042471.2:c.661+904C>A	NP_001035936.1:n.661+904C>A
NM_001165958.2:c.700+122C>A MANE Select	NP_001159430.1:n.700+122C>A
NM_001165959.2:c.700+122C>A	NP_001159431.1:n.700+122C>A
NM_001369402.2:c.661+904C>A	NP_001356331.1:n.661+904C>A
NM_001388420.1:c.700+122C>A	NP_001375349.1:n.700+122C>A
NM_001388421.1:c.700+122C>A	NP_001375350.1:n.700+122C>A
NM_001388422.1:c.661+904C>A	NP_001375351.1:n.661+904C>A
NM_001388423.1:c.661+904C>A	NP_001375352.1:n.661+904C>A
NM_001388424.1:c.576+1702C>A	NP_001375353.1:n.576+1702C>A
NM_018530.3:c.661+904C>A	NP_061000.2:n.661+904C>A
NR_170970.1:n.794+122C>A
NR_170971.1:n.1896-1067C>A
NR_170972.1:n.1812-1067C>A
NR_170973.1:n.2006+122C>A
NR_170974.1:n.1895+1702C>A