Canonical Allele Identifier: CA2622326180

Gene: SGCG

Linked Data

• gnomAD v4: 13-23181037-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23181037T>C , CM000675.2:g.23181037T>C	GRCh38
NC_000013.10:g.23755176T>C , CM000675.1:g.23755176T>C	GRCh37
NC_000013.9:g.22653176T>C	NCBI36
NG_008759.1:g.5117T>C , LRG_207:g.5117T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.-39T>C MANE Select	ENSP00000218867.3:n.-39T>C
ENST00000218867.3:c.-39T>C	ENSP00000218867.3:n.-39T>C
NM_000231.2:c.-39T>C , LRG_207t1:c.-39T>C	NP_000222.1:n.-39T>C
XM_005266505.2:c.-190T>C	XP_005266562.1:n.-190T>C
XM_006719861.2:c.54+20391T>C	XP_006719924.1:n.54+20391T>C
XM_006719861.3:c.54+20391T>C	XP_006719924.1:n.54+20391T>C
XM_024449397.1:c.-152+54T>C	XP_024305165.1:n.-152+54T>C
NM_000231.3:c.-39T>C MANE Select	NP_000222.2:n.-39T>C
NM_001378244.1:c.54+20391T>C	NP_001365173.1:n.54+20391T>C
NM_001378245.1:c.-152+54T>C	NP_001365174.1:n.-152+54T>C
NM_001378246.1:c.-190T>C	NP_001365175.1:n.-190T>C