Canonical Allele Identifier: CA798556703

Gene: SHROOM3

Linked Data

• dbSNP Id: rs1381854683
• gnomAD v3: 4-76476922-G-T
• gnomAD v4: 4-76476922-G-T
• MyVariant Identifiers: chr4:g.77398075G>T (hg19) ; chr4:g.76476922G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476922G>T , CM000666.2:g.76476922G>T	GRCh38
NC_000004.11:g.77398075G>T , CM000666.1:g.77398075G>T	GRCh37
NC_000004.10:g.77617099G>T	NCBI36
NG_028077.1:g.46823G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000296043.7:c.168+40702G>T MANE Select	ENSP00000296043.6:n.168+40702G>T
ENST00000296043.6:c.168+40702G>T	ENSP00000296043.6:n.168+40702G>T
ENST00000466541.1:n.75+40702G>T
ENST00000497440.5:n.109+40702G>T
NM_020859.3:c.168+40702G>T	NP_065910.3:n.168+40702G>T
XM_005263162.3:c.168+40702G>T	XP_005263219.1:n.168+40702G>T
XM_011532158.1:c.168+40702G>T	XP_011530460.1:n.168+40702G>T
XM_011532159.1:c.168+40702G>T	XP_011530461.1:n.168+40702G>T
XM_011532158.3:c.168+40702G>T	XP_011530460.1:n.168+40702G>T
NM_020859.4:c.168+40702G>T MANE Select	NP_065910.3:n.168+40702G>T