Canonical Allele Identifier: CA479446678

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48393721A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47999938A>G , CM000674.2:g.47999938A>G	GRCh38
NC_000012.11:g.48393721A>G , CM000674.1:g.48393721A>G	GRCh37
NC_000012.10:g.46679988A>G	NCBI36
NG_008072.1:g.9565T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.86-1507T>C	ENSP00000338213.6:n.86-1507T>C
ENST00000380518.8:c.273T>C MANE Select	ENSP00000369889.3:p.Thr91=
ENST00000490609.2:n.506T>C
ENST00000337299.6:c.86-1507T>C	ENSP00000338213.6:n.86-1507T>C
ENST00000380518.7:c.273T>C	ENSP00000369889.3:p.Thr91=
ENST00000474996.6:n.511T>C
ENST00000490609.1:n.438T>C
NM_001844.4:c.273T>C	NP_001835.3:p.Thr91=
NM_033150.2:c.86-1507T>C	NP_149162.2:n.86-1507T>C
XM_006719242.2:c.414T>C	XP_006719305.2:p.Thr138=
XM_011537928.1:c.414T>C	XP_011536230.1:p.Thr138=
XM_011537929.1:c.414T>C	XP_011536231.1:p.Thr138=
XM_011537930.1:c.414T>C	XP_011536232.1:p.Thr138=
XM_011537931.1:c.414T>C	XP_011536233.1:p.Thr138=
XM_011537932.1:c.414T>C	XP_011536234.1:p.Thr138=
XM_011537933.1:c.414T>C	XP_011536235.1:p.Thr138=
XM_011537934.1:c.414T>C	XP_011536236.1:p.Thr138=
XM_017018828.1:c.414T>C	XP_016874317.1:p.Thr138=
XM_017018829.1:c.414T>C	XP_016874318.1:p.Thr138=
XM_017018830.1:c.227-1507T>C	XP_016874319.1:n.227-1507T>C
XM_017018831.2:c.-274T>C	XP_016874320.1:n.-274T>C
NM_001844.5:c.273T>C MANE Select	NP_001835.3:p.Thr91=
NM_033150.3:c.86-1507T>C	NP_149162.2:n.86-1507T>C