Canonical Allele Identifier: CA2735643879

Gene: COMP

Linked Data

• dbSNP Id: rs1315181334

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785664C>A , CM000681.2:g.18785664C>A	GRCh38
NC_000019.9:g.18896474C>A , CM000681.1:g.18896474C>A	GRCh37
NC_000019.8:g.18757474C>A	NCBI36
NG_007070.1:g.10641G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1668+9G>T MANE Select	ENSP00000222271.2:n.1668+9G>T
ENST00000222271.6:c.1668+9G>T	ENSP00000222271.2:n.1668+9G>T
ENST00000425807.1:c.1509+9G>T	ENSP00000403792.1:n.1509+9G>T
ENST00000542601.6:c.1569+9G>T	ENSP00000439156.2:n.1569+9G>T
NM_000095.2:c.1668+9G>T	NP_000086.2:n.1668+9G>T
NM_000095.3:c.1668+9G>T MANE Select	NP_000086.2:n.1668+9G>T