Canonical Allele Identifier: CA506052349
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18895733A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18784923A>T , CM000681.2:g.18784923A>T GRCh38
NC_000019.9:g.18895733A>T , CM000681.1:g.18895733A>T GRCh37
NC_000019.8:g.18756733A>T NCBI36
NG_007070.1:g.11382T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1887T>A MANE Select ENSP00000222271.2:p.Ala629=
ENST00000222271.6:c.1887T>A ENSP00000222271.2:p.Ala629=
ENST00000425807.1:c.1728T>A ENSP00000403792.1:p.Ala576=
ENST00000542601.6:c.1788T>A ENSP00000439156.2:p.Ala596=
NM_000095.2:c.1887T>A NP_000086.2:p.Ala629=
NM_000095.3:c.1887T>A MANE Select NP_000086.2:p.Ala629=
Search 100 bp 5'
Search 100 bp 3'