Canonical Allele Identifier: CA2622326173

Gene: SGCG

Linked Data

• gnomAD v4: 13-23181019-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23181019G>T , CM000675.2:g.23181019G>T	GRCh38
NC_000013.10:g.23755158G>T , CM000675.1:g.23755158G>T	GRCh37
NC_000013.9:g.22653158G>T	NCBI36
NG_008759.1:g.5099G>T , LRG_207:g.5099G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218867.4:c.-57G>T MANE Select	ENSP00000218867.3:n.-57G>T
ENST00000218867.3:c.-57G>T	ENSP00000218867.3:n.-57G>T
NM_000231.2:c.-57G>T , LRG_207t1:c.-57G>T	NP_000222.1:n.-57G>T
XM_005266505.2:c.-208G>T	XP_005266562.1:n.-208G>T
XM_006719861.2:c.54+20373G>T	XP_006719924.1:n.54+20373G>T
XM_006719861.3:c.54+20373G>T	XP_006719924.1:n.54+20373G>T
XM_024449397.1:c.-152+36G>T	XP_024305165.1:n.-152+36G>T
NM_000231.3:c.-57G>T MANE Select	NP_000222.2:n.-57G>T
NM_001378244.1:c.54+20373G>T	NP_001365173.1:n.54+20373G>T
NM_001378245.1:c.-152+36G>T	NP_001365174.1:n.-152+36G>T
NM_001378246.1:c.-208G>T	NP_001365175.1:n.-208G>T