Canonical Allele Identifier: CA384541612

Gene: COL2A1

Linked Data

• dbSNP Id: rs1166535671
• gnomAD v2: 12-48372178-C-T
• gnomAD v4: 12-47978395-C-T
• MyVariant Identifiers: chr12:g.48372178C>T (hg19) ; chr12:g.47978395C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47978395C>T , CM000674.2:g.47978395C>T	GRCh38
NC_000012.11:g.48372178C>T , CM000674.1:g.48372178C>T	GRCh37
NC_000012.10:g.46658445C>T	NCBI36
NG_008072.1:g.31108G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.2692G>A	ENSP00000338213.6:p.Ala898Thr
ENST00000380518.8:c.2899G>A MANE Select	ENSP00000369889.3:p.Ala967Thr
ENST00000337299.6:c.2692G>A	ENSP00000338213.6:p.Ala898Thr
ENST00000380518.7:c.2899G>A	ENSP00000369889.3:p.Ala967Thr
ENST00000493991.5:n.1985G>A
NM_001844.4:c.2899G>A	NP_001835.3:p.Ala967Thr
NM_033150.2:c.2692G>A	NP_149162.2:p.Ala898Thr
XM_006719242.2:c.3043G>A	XP_006719305.2:p.Ala1015Thr
XM_011537928.1:c.3043G>A	XP_011536230.1:p.Ala1015Thr
XM_011537929.1:c.3043G>A	XP_011536231.1:p.Ala1015Thr
XM_011537930.1:c.3043G>A	XP_011536232.1:p.Ala1015Thr
XM_011537931.1:c.3043G>A	XP_011536233.1:p.Ala1015Thr
XM_011537932.1:c.3043G>A	XP_011536234.1:p.Ala1015Thr
XM_011537933.1:c.3043G>A	XP_011536235.1:p.Ala1015Thr
XM_011537934.1:c.3040G>A	XP_011536236.1:p.Ala1014Thr
XM_011537935.1:c.1987G>A	XP_011536237.1:p.Ala663Thr
XM_017018828.1:c.3043G>A	XP_016874317.1:p.Ala1015Thr
XM_017018829.1:c.3040G>A	XP_016874318.1:p.Ala1014Thr
XM_017018830.1:c.2833G>A	XP_016874319.1:p.Ala945Thr
XM_017018831.2:c.2353G>A	XP_016874320.1:p.Ala785Thr
NM_001844.5:c.2899G>A MANE Select	NP_001835.3:p.Ala967Thr
NM_033150.3:c.2692G>A	NP_149162.2:p.Ala898Thr