Canonical Allele Identifier: CA506117277

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896775T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785965T>G , CM000681.2:g.18785965T>G	GRCh38
NC_000019.9:g.18896775T>G , CM000681.1:g.18896775T>G	GRCh37
NC_000019.8:g.18757775T>G	NCBI36
NG_007070.1:g.10340A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1489A>C MANE Select	ENSP00000222271.2:p.Arg497=
ENST00000222271.6:c.1489A>C	ENSP00000222271.2:p.Arg497=
ENST00000425807.1:c.1330A>C	ENSP00000403792.1:p.Arg444=
ENST00000542601.6:c.1390A>C	ENSP00000439156.2:p.Arg464=
NM_000095.2:c.1489A>C	NP_000086.2:p.Arg497=
NM_000095.3:c.1489A>C MANE Select	NP_000086.2:p.Arg497=