Canonical Allele Identifier: CA506052834

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18897075T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786265T>C , CM000681.2:g.18786265T>C	GRCh38
NC_000019.9:g.18897075T>C , CM000681.1:g.18897075T>C	GRCh37
NC_000019.8:g.18758075T>C	NCBI36
NG_007070.1:g.10040A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1281A>G MANE Select	ENSP00000222271.2:p.Gly427=
ENST00000222271.6:c.1281A>G	ENSP00000222271.2:p.Gly427=
ENST00000425807.1:c.1122A>G	ENSP00000403792.1:p.Gly374=
ENST00000542601.6:c.1182A>G	ENSP00000439156.2:p.Gly394=
ENST00000612179.1:n.531A>G
NM_000095.2:c.1281A>G	NP_000086.2:p.Gly427=
NM_000095.3:c.1281A>G MANE Select	NP_000086.2:p.Gly427=