Canonical Allele Identifier: CA387501656

Gene: SGCG

Linked Data

• MyVariant Identifiers: chr13:g.23824836T>C (hg19) ; chr13:g.23250697T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23250697T>C , CM000675.2:g.23250697T>C	GRCh38
NC_000013.10:g.23824836T>C , CM000675.1:g.23824836T>C	GRCh37
NC_000013.9:g.22722836T>C	NCBI36
NG_008759.1:g.74777T>C , LRG_207:g.74777T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.365T>C MANE Select	ENSP00000218867.3:p.Val122Ala
ENST00000218867.3:c.365T>C	ENSP00000218867.3:p.Val122Ala
NM_000231.2:c.365T>C , LRG_207t1:c.365T>C	NP_000222.1:p.Val122Ala
XM_005266505.2:c.365T>C	XP_005266562.1:p.Val122Ala
XM_006719861.2:c.419T>C	XP_006719924.1:p.Val140Ala
XM_006719861.3:c.419T>C	XP_006719924.1:p.Val140Ala
XM_024449397.1:c.365T>C	XP_024305165.1:p.Val122Ala
NM_000231.3:c.365T>C MANE Select	NP_000222.2:p.Val122Ala
NM_001378244.1:c.419T>C	NP_001365173.1:p.Val140Ala
NM_001378245.1:c.365T>C	NP_001365174.1:p.Val122Ala
NM_001378246.1:c.365T>C	NP_001365175.1:p.Val122Ala