Canonical Allele Identifier: CA8536227
Gene: GSDMB HGNC NCBI

Linked Data

dbSNP Id: rs2305480

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39905943G>A , CM000679.2:g.39905943G>A GRCh38
NC_000017.10:g.38062196G>A , CM000679.1:g.38062196G>A GRCh37
NC_000017.9:g.35315722G>A NCBI36
NG_015804.1:g.17708C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000418519.6:c.931C>T MANE Select ENSP00000415049.1:p.Pro311Ser
ENST00000309481.11:c.892C>T ENSP00000312584.7:p.Pro298Ser
ENST00000360317.7:c.931C>T ENSP00000353465.3:p.Pro311Ser
ENST00000394175.6:c.865C>T ENSP00000377729.2:p.Pro289Ser
ENST00000394179.5:c.892C>T ENSP00000377733.2:p.Pro298Ser
ENST00000418519.5:c.931C>T ENSP00000415049.1:p.Pro311Ser
ENST00000477054.6:n.4119C>T
ENST00000479136.5:n.1672C>T
ENST00000520542.5:c.904C>T ENSP00000430157.1:p.Pro302Ser
ENST00000522564.5:c.638C>T ENSP00000428217.1:n.638C>T
ENST00000523371.5:c.807C>T ENSP00000429265.1:n.807C>T
ENST00000524039.5:c.780C>T ENSP00000428712.1:n.780C>T
NM_001042471.1:c.892C>T NP_001035936.1:p.Pro298Ser
NM_001165958.1:c.931C>T NP_001159430.1:p.Pro311Ser
NM_001165959.1:c.904C>T NP_001159431.1:p.Pro302Ser
NM_018530.2:c.865C>T NP_061000.2:p.Pro289Ser
XM_011525001.1:c.943C>T XP_011523303.1:p.Pro315Ser
XM_011525002.1:c.943C>T XP_011523304.1:p.Pro315Ser
XM_011525003.1:c.943C>T XP_011523305.1:p.Pro315Ser
XM_011525004.1:c.943C>T XP_011523306.1:p.Pro315Ser
XM_011525005.1:c.943C>T XP_011523307.1:p.Pro315Ser
XM_011525006.1:c.943C>T XP_011523308.1:p.Pro315Ser
XM_011525007.1:c.943C>T XP_011523309.1:p.Pro315Ser
XM_011525008.1:c.943C>T XP_011523310.1:p.Pro315Ser
XM_011525009.1:c.943C>T XP_011523311.1:p.Pro315Ser
XM_011525010.1:c.943C>T XP_011523312.1:p.Pro315Ser
XM_011525011.1:c.943C>T XP_011523313.1:p.Pro315Ser
XM_011525012.1:c.943C>T XP_011523314.1:p.Pro315Ser
XM_011525013.1:c.943C>T XP_011523315.1:p.Pro315Ser
XM_011525014.1:c.943C>T XP_011523316.1:p.Pro315Ser
XM_011525015.1:c.943C>T XP_011523317.1:p.Pro315Ser
XM_011525016.1:c.931C>T XP_011523318.1:p.Pro311Ser
XM_011525017.1:c.916C>T XP_011523319.1:p.Pro306Ser
XM_011525018.1:c.904C>T XP_011523320.1:p.Pro302Ser
XM_011525019.1:c.892C>T XP_011523321.1:p.Pro298Ser
XM_011525020.1:c.865C>T XP_011523322.1:p.Pro289Ser
XR_934504.1:n.2504C>T
NM_001369402.1:c.892C>T NP_001356331.1:p.Pro298Ser
NM_001042471.2:c.892C>T NP_001035936.1:p.Pro298Ser
NM_001165958.2:c.931C>T MANE Select NP_001159430.1:p.Pro311Ser
NM_001165959.2:c.904C>T NP_001159431.1:p.Pro302Ser
NM_001369402.2:c.892C>T NP_001356331.1:p.Pro298Ser
NM_001388420.1:c.931C>T NP_001375349.1:p.Pro311Ser
NM_001388421.1:c.904C>T NP_001375350.1:p.Pro302Ser
NM_001388422.1:c.892C>T NP_001375351.1:p.Pro298Ser
NM_001388423.1:c.865C>T NP_001375352.1:p.Pro289Ser
NM_001388424.1:c.619C>T NP_001375353.1:p.Pro207Ser
NM_018530.3:c.865C>T NP_061000.2:p.Pro289Ser
NR_170970.1:n.1025C>T
NR_170971.1:n.2126C>T
NR_170972.1:n.2042C>T
NR_170973.1:n.2237C>T
NR_170974.1:n.2099C>T