Canonical Allele Identifier: CA506117476

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896887T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786077T>G , CM000681.2:g.18786077T>G	GRCh38
NC_000019.9:g.18896887T>G , CM000681.1:g.18896887T>G	GRCh37
NC_000019.8:g.18757887T>G	NCBI36
NG_007070.1:g.10228A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1377A>C MANE Select	ENSP00000222271.2:p.Ser459=
ENST00000222271.6:c.1377A>C	ENSP00000222271.2:p.Ser459=
ENST00000425807.1:c.1218A>C	ENSP00000403792.1:p.Ser406=
ENST00000542601.6:c.1278A>C	ENSP00000439156.2:p.Ser426=
NM_000095.2:c.1377A>C	NP_000086.2:p.Ser459=
NM_000095.3:c.1377A>C MANE Select	NP_000086.2:p.Ser459=