Canonical Allele Identifier: CA506117325
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18896522A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785712A>T , CM000681.2:g.18785712A>T GRCh38
NC_000019.9:g.18896522A>T , CM000681.1:g.18896522A>T GRCh37
NC_000019.8:g.18757522A>T NCBI36
NG_007070.1:g.10593T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1629T>A MANE Select ENSP00000222271.2:p.Gly543=
ENST00000222271.6:c.1629T>A ENSP00000222271.2:p.Gly543=
ENST00000425807.1:c.1470T>A ENSP00000403792.1:p.Gly490=
ENST00000542601.6:c.1530T>A ENSP00000439156.2:p.Gly510=
NM_000095.2:c.1629T>A NP_000086.2:p.Gly543=
NM_000095.3:c.1629T>A MANE Select NP_000086.2:p.Gly543=
Search 100 bp 5'
Search 100 bp 3'