Canonical Allele Identifier: CA506053386

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18900041C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789232C>T , CM000681.2:g.18789232C>T	GRCh38
NC_000019.9:g.18900041C>T , CM000681.1:g.18900041C>T	GRCh37
NC_000019.8:g.18761041C>T	NCBI36
NG_007070.1:g.7074G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.456G>A MANE Select	ENSP00000222271.2:p.Glu152=
ENST00000222271.6:c.456G>A	ENSP00000222271.2:p.Glu152=
ENST00000425807.1:c.391-340G>A	ENSP00000403792.1:n.391-340G>A
ENST00000542601.6:c.357G>A	ENSP00000439156.2:p.Glu119=
NM_000095.2:c.456G>A	NP_000086.2:p.Glu152=
NM_000095.3:c.456G>A MANE Select	NP_000086.2:p.Glu152=