Canonical Allele Identifier: CA506053058
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18898322G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787513G>A , CM000681.2:g.18787513G>A GRCh38
NC_000019.9:g.18898322G>A , CM000681.1:g.18898322G>A GRCh37
NC_000019.8:g.18759322G>A NCBI36
NG_007070.1:g.8793C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1113C>T MANE Select ENSP00000222271.2:p.Cys371=
ENST00000222271.6:c.1113C>T ENSP00000222271.2:p.Cys371=
ENST00000425807.1:c.954C>T ENSP00000403792.1:p.Cys318=
ENST00000542601.6:c.1014C>T ENSP00000439156.2:p.Cys338=
NM_000095.2:c.1113C>T NP_000086.2:p.Cys371=
NM_000095.3:c.1113C>T MANE Select NP_000086.2:p.Cys371=