Canonical Allele Identifier: CA9316360
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs753703511

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785790G>A , CM000681.2:g.18785790G>A GRCh38
NC_000019.9:g.18896600G>A , CM000681.1:g.18896600G>A GRCh37
NC_000019.8:g.18757600G>A NCBI36
NG_007070.1:g.10515C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1551C>T MANE Select ENSP00000222271.2:p.Ile517=
ENST00000222271.6:c.1551C>T ENSP00000222271.2:p.Ile517=
ENST00000425807.1:c.1392C>T ENSP00000403792.1:p.Ile464=
ENST00000542601.6:c.1452C>T ENSP00000439156.2:p.Ile484=
NM_000095.2:c.1551C>T NP_000086.2:p.Ile517=
NM_000095.3:c.1551C>T MANE Select NP_000086.2:p.Ile517=