Canonical Allele Identifier: CA506052714
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18896926G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786116G>A , CM000681.2:g.18786116G>A GRCh38
NC_000019.9:g.18896926G>A , CM000681.1:g.18896926G>A GRCh37
NC_000019.8:g.18757926G>A NCBI36
NG_007070.1:g.10189C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1338C>T MANE Select ENSP00000222271.2:p.Asp446=
ENST00000222271.6:c.1338C>T ENSP00000222271.2:p.Asp446=
ENST00000425807.1:c.1179C>T ENSP00000403792.1:p.Asp393=
ENST00000542601.6:c.1239C>T ENSP00000439156.2:p.Asp413=
NM_000095.2:c.1338C>T NP_000086.2:p.Asp446=
NM_000095.3:c.1338C>T MANE Select NP_000086.2:p.Asp446=