Canonical Allele Identifier: CA506117242

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896654G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785844G>C , CM000681.2:g.18785844G>C	GRCh38
NC_000019.9:g.18896654G>C , CM000681.1:g.18896654G>C	GRCh37
NC_000019.8:g.18757654G>C	NCBI36
NG_007070.1:g.10461C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1497C>G MANE Select	ENSP00000222271.2:p.Gly499=
ENST00000222271.6:c.1497C>G	ENSP00000222271.2:p.Gly499=
ENST00000425807.1:c.1338C>G	ENSP00000403792.1:p.Gly446=
ENST00000542601.6:c.1398C>G	ENSP00000439156.2:p.Gly466=
NM_000095.2:c.1497C>G	NP_000086.2:p.Gly499=
NM_000095.3:c.1497C>G MANE Select	NP_000086.2:p.Gly499=