Canonical Allele Identifier: CA506053392

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18900053C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789244C>G , CM000681.2:g.18789244C>G	GRCh38
NC_000019.9:g.18900053C>G , CM000681.1:g.18900053C>G	GRCh37
NC_000019.8:g.18761053C>G	NCBI36
NG_007070.1:g.7062G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.444G>C MANE Select	ENSP00000222271.2:p.Gly148=
ENST00000222271.6:c.444G>C	ENSP00000222271.2:p.Gly148=
ENST00000425807.1:c.391-352G>C	ENSP00000403792.1:n.391-352G>C
ENST00000542601.6:c.345G>C	ENSP00000439156.2:p.Gly115=
NM_000095.2:c.444G>C	NP_000086.2:p.Gly148=
NM_000095.3:c.444G>C MANE Select	NP_000086.2:p.Gly148=