Canonical Allele Identifier: CA506052495
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18895883G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785073G>T , CM000681.2:g.18785073G>T GRCh38
NC_000019.9:g.18895883G>T , CM000681.1:g.18895883G>T GRCh37
NC_000019.8:g.18756883G>T NCBI36
NG_007070.1:g.11232C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1737C>A MANE Select ENSP00000222271.2:p.Gly579=
ENST00000222271.6:c.1737C>A ENSP00000222271.2:p.Gly579=
ENST00000425807.1:c.1578C>A ENSP00000403792.1:p.Gly526=
ENST00000542601.6:c.1638C>A ENSP00000439156.2:p.Gly546=
NM_000095.2:c.1737C>A NP_000086.2:p.Gly579=
NM_000095.3:c.1737C>A MANE Select NP_000086.2:p.Gly579=