Canonical Allele Identifier: CA6909564

Gene: SGCG

Linked Data

• dbSNP Id: rs780186997
• ExAC: 13:23777929 A / G
• gnomAD v2: 13-23777929-A-G
• gnomAD v4: 13-23203790-A-G
• MyVariant Identifiers: chr13:g.23777929A>G (hg19) ; chr13:g.23203790A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23203790A>G , CM000675.2:g.23203790A>G	GRCh38
NC_000013.10:g.23777929A>G , CM000675.1:g.23777929A>G	GRCh37
NC_000013.9:g.22675929A>G	NCBI36
NG_008759.1:g.27870A>G , LRG_207:g.27870A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218867.4:c.96A>G MANE Select	ENSP00000218867.3:p.Arg32=
ENST00000218867.3:c.96A>G	ENSP00000218867.3:p.Arg32=
NM_000231.2:c.96A>G , LRG_207t1:c.96A>G	NP_000222.1:p.Arg32=
XM_005266505.2:c.96A>G	XP_005266562.1:p.Arg32=
XM_006719861.2:c.150A>G	XP_006719924.1:p.Arg50=
XM_006719861.3:c.150A>G	XP_006719924.1:p.Arg50=
XM_024449397.1:c.96A>G	XP_024305165.1:p.Arg32=
NM_000231.3:c.96A>G MANE Select	NP_000222.2:p.Arg32=
NM_001378244.1:c.150A>G	NP_001365173.1:p.Arg50=
NM_001378245.1:c.96A>G	NP_001365174.1:p.Arg32=
NM_001378246.1:c.96A>G	NP_001365175.1:p.Arg32=