Canonical Allele Identifier: CA387502559

Gene: SGCG

Linked Data

• MyVariant Identifiers: chr13:g.23777936T>C (hg19) ; chr13:g.23203797T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23203797T>C , CM000675.2:g.23203797T>C	GRCh38
NC_000013.10:g.23777936T>C , CM000675.1:g.23777936T>C	GRCh37
NC_000013.9:g.22675936T>C	NCBI36
NG_008759.1:g.27877T>C , LRG_207:g.27877T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218867.4:c.103T>C MANE Select	ENSP00000218867.3:p.Cys35Arg
ENST00000218867.3:c.103T>C	ENSP00000218867.3:p.Cys35Arg
NM_000231.2:c.103T>C , LRG_207t1:c.103T>C	NP_000222.1:p.Cys35Arg
XM_005266505.2:c.103T>C	XP_005266562.1:p.Cys35Arg
XM_006719861.2:c.157T>C	XP_006719924.1:p.Cys53Arg
XM_006719861.3:c.157T>C	XP_006719924.1:p.Cys53Arg
XM_024449397.1:c.103T>C	XP_024305165.1:p.Cys35Arg
NM_000231.3:c.103T>C MANE Select	NP_000222.2:p.Cys35Arg
NM_001378244.1:c.157T>C	NP_001365173.1:p.Cys53Arg
NM_001378245.1:c.103T>C	NP_001365174.1:p.Cys35Arg
NM_001378246.1:c.103T>C	NP_001365175.1:p.Cys35Arg