Canonical Allele Identifier: CA479452326
Gene: COL2A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.48370640C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47976857C>T , CM000674.2:g.47976857C>T GRCh38
NC_000012.11:g.48370640C>T , CM000674.1:g.48370640C>T GRCh37
NC_000012.10:g.46656907C>T NCBI36
NG_008072.1:g.32646G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000337299.7:c.3183G>A ENSP00000338213.6:p.Lys1061=
ENST00000380518.8:c.3390G>A MANE Select ENSP00000369889.3:p.Lys1130=
ENST00000337299.6:c.3183G>A ENSP00000338213.6:p.Lys1061=
ENST00000380518.7:c.3390G>A ENSP00000369889.3:p.Lys1130=
ENST00000493991.5:n.2476G>A
ENST00000546974.1:n.243G>A
NM_001844.4:c.3390G>A NP_001835.3:p.Lys1130=
NM_033150.2:c.3183G>A NP_149162.2:p.Lys1061=
XM_006719242.2:c.3534G>A XP_006719305.2:p.Lys1178=
XM_011537928.1:c.3534G>A XP_011536230.1:p.Lys1178=
XM_011537929.1:c.3534G>A XP_011536231.1:p.Lys1178=
XM_011537930.1:c.3534G>A XP_011536232.1:p.Lys1178=
XM_011537931.1:c.3534G>A XP_011536233.1:p.Lys1178=
XM_011537932.1:c.3534G>A XP_011536234.1:p.Lys1178=
XM_011537933.1:c.3534G>A XP_011536235.1:p.Lys1178=
XM_011537934.1:c.3531G>A XP_011536236.1:p.Lys1177=
XM_011537935.1:c.2478G>A XP_011536237.1:p.Lys826=
XM_017018828.1:c.3534G>A XP_016874317.1:p.Lys1178=
XM_017018829.1:c.3531G>A XP_016874318.1:p.Lys1177=
XM_017018830.1:c.3324G>A XP_016874319.1:p.Lys1108=
XM_017018831.2:c.2844G>A XP_016874320.1:p.Lys948=
NM_001844.5:c.3390G>A MANE Select NP_001835.3:p.Lys1130=
NM_033150.3:c.3183G>A NP_149162.2:p.Lys1061=