Canonical Allele Identifier: CA479697087

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48369374A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47975591A>G , CM000674.2:g.47975591A>G	GRCh38
NC_000012.11:g.48369374A>G , CM000674.1:g.48369374A>G	GRCh37
NC_000012.10:g.46655641A>G	NCBI36
NG_008072.1:g.33912T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.3405T>C	ENSP00000338213.6:p.Asn1135=
ENST00000380518.8:c.3612T>C MANE Select	ENSP00000369889.3:p.Asn1204=
ENST00000337299.6:c.3405T>C	ENSP00000338213.6:p.Asn1135=
ENST00000380518.7:c.3612T>C	ENSP00000369889.3:p.Asn1204=
ENST00000493991.5:n.2698T>C
ENST00000546974.1:n.465T>C
NM_001844.4:c.3612T>C	NP_001835.3:p.Asn1204=
NM_033150.2:c.3405T>C	NP_149162.2:p.Asn1135=
XM_006719242.2:c.3756T>C	XP_006719305.2:p.Asn1252=
XM_011537928.1:c.3756T>C	XP_011536230.1:p.Asn1252=
XM_011537929.1:c.3756T>C	XP_011536231.1:p.Asn1252=
XM_011537930.1:c.3756T>C	XP_011536232.1:p.Asn1252=
XM_011537931.1:c.3756T>C	XP_011536233.1:p.Asn1252=
XM_011537932.1:c.3756T>C	XP_011536234.1:p.Asn1252=
XM_011537933.1:c.3756T>C	XP_011536235.1:p.Asn1252=
XM_011537934.1:c.3753T>C	XP_011536236.1:p.Asn1251=
XM_011537935.1:c.2700T>C	XP_011536237.1:p.Asn900=
XM_017018828.1:c.3756T>C	XP_016874317.1:p.Asn1252=
XM_017018829.1:c.3753T>C	XP_016874318.1:p.Asn1251=
XM_017018830.1:c.3546T>C	XP_016874319.1:p.Asn1182=
XM_017018831.2:c.3066T>C	XP_016874320.1:p.Asn1022=
NM_001844.5:c.3612T>C MANE Select	NP_001835.3:p.Asn1204=
NM_033150.3:c.3405T>C	NP_149162.2:p.Asn1135=