Canonical Allele Identifier: CA1139771742
Gene: COL2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17362
ClinVar RCV Id: RCV000018906
dbSNP Id: rs2136609285

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47993807_47993834del , CM000674.2:g.47993807_47993834del GRCh38
NC_000012.11:g.48387590_48387617del , CM000674.1:g.48387590_48387617del GRCh37
NC_000012.10:g.46673857_46673884del NCBI36
NG_008072.1:g.15676_15703del

Transcript Alleles

HGVS Amino-acid change
ENST00000337299.7:c.699_717+9del
ENST00000380518.8:c.906_924+9del
ENST00000337299.6:c.699_717+9del
ENST00000380518.7:c.906_924+9del
NM_001844.4:c.906_924+9del
NM_033150.2:c.699_717+9del
XM_006719242.2:c.1050_1068+9del
XM_011537928.1:c.1050_1068+9del
XM_011537929.1:c.1050_1068+9del
XM_011537930.1:c.1050_1068+9del
XM_011537931.1:c.1050_1068+9del
XM_011537932.1:c.1050_1068+9del
XM_011537933.1:c.1050_1068+9del
XM_011537934.1:c.1047_1065+9del
XM_017018828.1:c.1050_1068+9del
XM_017018829.1:c.1047_1065+9del
XM_017018830.1:c.840_858+9del
XM_017018831.2:c.360_378+9del
NM_001844.5:c.906_924+9del
NM_033150.3:c.699_717+9del