Canonical Allele Identifier: CA479440515

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48387610C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47993827C>G , CM000674.2:g.47993827C>G	GRCh38
NC_000012.11:g.48387610C>G , CM000674.1:g.48387610C>G	GRCh37
NC_000012.10:g.46673877C>G	NCBI36
NG_008072.1:g.15676G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.699G>C	ENSP00000338213.6:p.Ala233=
ENST00000380518.8:c.906G>C MANE Select	ENSP00000369889.3:p.Ala302=
ENST00000337299.6:c.699G>C	ENSP00000338213.6:p.Ala233=
ENST00000380518.7:c.906G>C	ENSP00000369889.3:p.Ala302=
NM_001844.4:c.906G>C	NP_001835.3:p.Ala302=
NM_033150.2:c.699G>C	NP_149162.2:p.Ala233=
XM_006719242.2:c.1050G>C	XP_006719305.2:p.Ala350=
XM_011537928.1:c.1050G>C	XP_011536230.1:p.Ala350=
XM_011537929.1:c.1050G>C	XP_011536231.1:p.Ala350=
XM_011537930.1:c.1050G>C	XP_011536232.1:p.Ala350=
XM_011537931.1:c.1050G>C	XP_011536233.1:p.Ala350=
XM_011537932.1:c.1050G>C	XP_011536234.1:p.Ala350=
XM_011537933.1:c.1050G>C	XP_011536235.1:p.Ala350=
XM_011537934.1:c.1047G>C	XP_011536236.1:p.Ala349=
XM_017018828.1:c.1050G>C	XP_016874317.1:p.Ala350=
XM_017018829.1:c.1047G>C	XP_016874318.1:p.Ala349=
XM_017018830.1:c.840G>C	XP_016874319.1:p.Ala280=
XM_017018831.2:c.360G>C	XP_016874320.1:p.Ala120=
NM_001844.5:c.906G>C MANE Select	NP_001835.3:p.Ala302=
NM_033150.3:c.699G>C	NP_149162.2:p.Ala233=