Canonical Allele Identifier: CA404875041

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18893939G>C (hg19) ; chr19:g.18783129G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18783129G>C , CM000681.2:g.18783129G>C	GRCh38
NC_000019.9:g.18893939G>C , CM000681.1:g.18893939G>C	GRCh37
NC_000019.8:g.18754939G>C	NCBI36
NG_007070.1:g.13176C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.2152C>G MANE Select	ENSP00000222271.2:p.Arg718Gly
ENST00000222271.6:c.2152C>G	ENSP00000222271.2:p.Arg718Gly
ENST00000425807.1:c.1993C>G	ENSP00000403792.1:p.Arg665Gly
ENST00000542601.6:c.2053C>G	ENSP00000439156.2:p.Arg685Gly
NM_000095.2:c.2152C>G	NP_000086.2:p.Arg718Gly
NM_000095.3:c.2152C>G MANE Select	NP_000086.2:p.Arg718Gly