Canonical Allele Identifier: CA404888649
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787608C>G , CM000681.2:g.18787608C>G GRCh38
NC_000019.9:g.18898417C>G , CM000681.1:g.18898417C>G GRCh37
NC_000019.8:g.18759417C>G NCBI36
NG_007070.1:g.8698G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1018G>C MANE Select ENSP00000222271.2:p.Asp340His
ENST00000222271.6:c.1018G>C ENSP00000222271.2:p.Asp340His
ENST00000425807.1:c.859G>C ENSP00000403792.1:p.Asp287His
ENST00000542601.6:c.919G>C ENSP00000439156.2:p.Asp307His
NM_000095.2:c.1018G>C NP_000086.2:p.Asp340His
NM_000095.3:c.1018G>C MANE Select NP_000086.2:p.Asp340His