Canonical Allele Identifier: CA6536083
Gene: COL2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 839519
ClinVar RCV Id: RCV001041293
dbSNP Id: rs776744207

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48000054G>A , CM000674.2:g.48000054G>A GRCh38
NC_000012.11:g.48393837G>A , CM000674.1:g.48393837G>A GRCh37
NC_000012.10:g.46680104G>A NCBI36
NG_008072.1:g.9449C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000337299.7:c.86-1623C>T ENSP00000338213.6:n.86-1623C>T
ENST00000380518.8:c.157C>T MANE Select ENSP00000369889.3:p.Arg53Trp
ENST00000490609.2:n.390C>T
ENST00000337299.6:c.86-1623C>T ENSP00000338213.6:n.86-1623C>T
ENST00000380518.7:c.157C>T ENSP00000369889.3:p.Arg53Trp
ENST00000474996.6:n.395C>T
ENST00000490609.1:n.322C>T
NM_001844.4:c.157C>T NP_001835.3:p.Arg53Trp
NM_033150.2:c.86-1623C>T NP_149162.2:n.86-1623C>T
XM_006719242.2:c.298C>T XP_006719305.2:p.Arg100Trp
XM_011537928.1:c.298C>T XP_011536230.1:p.Arg100Trp
XM_011537929.1:c.298C>T XP_011536231.1:p.Arg100Trp
XM_011537930.1:c.298C>T XP_011536232.1:p.Arg100Trp
XM_011537931.1:c.298C>T XP_011536233.1:p.Arg100Trp
XM_011537932.1:c.298C>T XP_011536234.1:p.Arg100Trp
XM_011537933.1:c.298C>T XP_011536235.1:p.Arg100Trp
XM_011537934.1:c.298C>T XP_011536236.1:p.Arg100Trp
XM_017018828.1:c.298C>T XP_016874317.1:p.Arg100Trp
XM_017018829.1:c.298C>T XP_016874318.1:p.Arg100Trp
XM_017018830.1:c.227-1623C>T XP_016874319.1:n.227-1623C>T
XM_017018831.2:c.-390C>T XP_016874320.1:n.-390C>T
NM_001844.5:c.157C>T MANE Select NP_001835.3:p.Arg53Trp
NM_033150.3:c.86-1623C>T NP_149162.2:n.86-1623C>T