Canonical Allele Identifier: CA608612016

Gene: SGCG

Linked Data

• dbSNP Id: rs1309644913
• gnomAD v2: 13-23824728-A-C
• gnomAD v4: 13-23250589-A-C
• MyVariant Identifiers: chr13:g.23824728A>C (hg19) ; chr13:g.23250589A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23250589A>C , CM000675.2:g.23250589A>C	GRCh38
NC_000013.10:g.23824728A>C , CM000675.1:g.23824728A>C	GRCh37
NC_000013.9:g.22722728A>C	NCBI36
NG_008759.1:g.74669A>C , LRG_207:g.74669A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.298-41A>C MANE Select	ENSP00000218867.3:n.298-41A>C
ENST00000218867.3:c.298-41A>C	ENSP00000218867.3:n.298-41A>C
NM_000231.2:c.298-41A>C , LRG_207t1:c.298-41A>C	NP_000222.1:n.298-41A>C
XM_005266505.2:c.298-41A>C	XP_005266562.1:n.298-41A>C
XM_006719861.2:c.352-41A>C	XP_006719924.1:n.352-41A>C
XM_006719861.3:c.352-41A>C	XP_006719924.1:n.352-41A>C
XM_024449397.1:c.298-41A>C	XP_024305165.1:n.298-41A>C
NM_000231.3:c.298-41A>C MANE Select	NP_000222.2:n.298-41A>C
NM_001378244.1:c.352-41A>C	NP_001365173.1:n.352-41A>C
NM_001378245.1:c.298-41A>C	NP_001365174.1:n.298-41A>C
NM_001378246.1:c.298-41A>C	NP_001365175.1:n.298-41A>C