Canonical Allele Identifier: CA281742

Gene: COL2A1

Linked Data

• ClinVar Variation Id: 17360
• ClinVar RCV Id: RCV000018904 ; RCV000579130
• dbSNP Id: rs121912869
• gnomAD v4: 12-47995904-G-A
• MyVariant Identifiers: chr12:g.48389687G>A (hg19) ; chr12:g.47995904G>A (hg38)
• PubMed: PMID:2803268 ; PMID:8434604

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47995904G>A , CM000674.2:g.47995904G>A	GRCh38
NC_000012.11:g.48389687G>A , CM000674.1:g.48389687G>A	GRCh37
NC_000012.10:g.46675954G>A	NCBI36
NG_008072.1:g.13599C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.418C>T	ENSP00000338213.6:p.Arg140Ter
ENST00000380518.8:c.625C>T MANE Select	ENSP00000369889.3:p.Arg209Ter
ENST00000337299.6:c.418C>T	ENSP00000338213.6:p.Arg140Ter
ENST00000380518.7:c.625C>T	ENSP00000369889.3:p.Arg209Ter
NM_001844.4:c.625C>T	NP_001835.3:p.Arg209Ter
NM_033150.2:c.418C>T	NP_149162.2:p.Arg140Ter
XM_006719242.2:c.769C>T	XP_006719305.2:p.Arg257Ter
XM_011537928.1:c.769C>T	XP_011536230.1:p.Arg257Ter
XM_011537929.1:c.769C>T	XP_011536231.1:p.Arg257Ter
XM_011537930.1:c.769C>T	XP_011536232.1:p.Arg257Ter
XM_011537931.1:c.769C>T	XP_011536233.1:p.Arg257Ter
XM_011537932.1:c.769C>T	XP_011536234.1:p.Arg257Ter
XM_011537933.1:c.769C>T	XP_011536235.1:p.Arg257Ter
XM_011537934.1:c.766C>T	XP_011536236.1:p.Arg256Ter
XM_017018828.1:c.769C>T	XP_016874317.1:p.Arg257Ter
XM_017018829.1:c.766C>T	XP_016874318.1:p.Arg256Ter
XM_017018830.1:c.559C>T	XP_016874319.1:p.Arg187Ter
XM_017018831.2:c.79C>T	XP_016874320.1:p.Arg27Ter
NM_001844.5:c.625C>T MANE Select	NP_001835.3:p.Arg209Ter
NM_033150.3:c.418C>T	NP_149162.2:p.Arg140Ter