Canonical Allele Identifier: CA479442076

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48389664A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47995881A>T , CM000674.2:g.47995881A>T	GRCh38
NC_000012.11:g.48389664A>T , CM000674.1:g.48389664A>T	GRCh37
NC_000012.10:g.46675931A>T	NCBI36
NG_008072.1:g.13622T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.441T>A	ENSP00000338213.6:p.Gly147=
ENST00000380518.8:c.648T>A MANE Select	ENSP00000369889.3:p.Gly216=
ENST00000337299.6:c.441T>A	ENSP00000338213.6:p.Gly147=
ENST00000380518.7:c.648T>A	ENSP00000369889.3:p.Gly216=
NM_001844.4:c.648T>A	NP_001835.3:p.Gly216=
NM_033150.2:c.441T>A	NP_149162.2:p.Gly147=
XM_006719242.2:c.792T>A	XP_006719305.2:p.Gly264=
XM_011537928.1:c.792T>A	XP_011536230.1:p.Gly264=
XM_011537929.1:c.792T>A	XP_011536231.1:p.Gly264=
XM_011537930.1:c.792T>A	XP_011536232.1:p.Gly264=
XM_011537931.1:c.792T>A	XP_011536233.1:p.Gly264=
XM_011537932.1:c.792T>A	XP_011536234.1:p.Gly264=
XM_011537933.1:c.792T>A	XP_011536235.1:p.Gly264=
XM_011537934.1:c.789T>A	XP_011536236.1:p.Gly263=
XM_017018828.1:c.792T>A	XP_016874317.1:p.Gly264=
XM_017018829.1:c.789T>A	XP_016874318.1:p.Gly263=
XM_017018830.1:c.582T>A	XP_016874319.1:p.Gly194=
XM_017018831.2:c.102T>A	XP_016874320.1:p.Gly34=
NM_001844.5:c.648T>A MANE Select	NP_001835.3:p.Gly216=
NM_033150.3:c.441T>A	NP_149162.2:p.Gly147=