Canonical Allele Identifier: CA384540524

Gene: COL2A1

Linked Data

• ClinVar Variation Id: 501233
• ClinVar RCV Id: RCV000593974 ; RCV001822860
• dbSNP Id: rs1555165242
• MyVariant Identifiers: chr12:g.48371399C>T (hg19) ; chr12:g.47977616C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47977616C>T , CM000674.2:g.47977616C>T	GRCh38
NC_000012.11:g.48371399C>T , CM000674.1:g.48371399C>T	GRCh37
NC_000012.10:g.46657666C>T	NCBI36
NG_008072.1:g.31887G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.2942G>A	ENSP00000338213.6:p.Gly981Asp
ENST00000380518.8:c.3149G>A MANE Select	ENSP00000369889.3:p.Gly1050Asp
ENST00000337299.6:c.2942G>A	ENSP00000338213.6:p.Gly981Asp
ENST00000380518.7:c.3149G>A	ENSP00000369889.3:p.Gly1050Asp
ENST00000493991.5:n.2235G>A
NM_001844.4:c.3149G>A	NP_001835.3:p.Gly1050Asp
NM_033150.2:c.2942G>A	NP_149162.2:p.Gly981Asp
XM_006719242.2:c.3293G>A	XP_006719305.2:p.Gly1098Asp
XM_011537928.1:c.3293G>A	XP_011536230.1:p.Gly1098Asp
XM_011537929.1:c.3293G>A	XP_011536231.1:p.Gly1098Asp
XM_011537930.1:c.3293G>A	XP_011536232.1:p.Gly1098Asp
XM_011537931.1:c.3293G>A	XP_011536233.1:p.Gly1098Asp
XM_011537932.1:c.3293G>A	XP_011536234.1:p.Gly1098Asp
XM_011537933.1:c.3293G>A	XP_011536235.1:p.Gly1098Asp
XM_011537934.1:c.3290G>A	XP_011536236.1:p.Gly1097Asp
XM_011537935.1:c.2237G>A	XP_011536237.1:p.Gly746Asp
XM_017018828.1:c.3293G>A	XP_016874317.1:p.Gly1098Asp
XM_017018829.1:c.3290G>A	XP_016874318.1:p.Gly1097Asp
XM_017018830.1:c.3083G>A	XP_016874319.1:p.Gly1028Asp
XM_017018831.2:c.2603G>A	XP_016874320.1:p.Gly868Asp
NM_001844.5:c.3149G>A MANE Select	NP_001835.3:p.Gly1050Asp
NM_033150.3:c.2942G>A	NP_149162.2:p.Gly981Asp