Canonical Allele Identifier: CA2576725653
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18783039T>A , CM000681.2:g.18783039T>A GRCh38
NC_000019.9:g.18893849T>A , CM000681.1:g.18893849T>A GRCh37
NC_000019.8:g.18754849T>A NCBI36
NG_007070.1:g.13266A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.2227+15A>T MANE Select ENSP00000222271.2:n.2227+15A>T
ENST00000222271.6:c.2227+15A>T ENSP00000222271.2:n.2227+15A>T
ENST00000425807.1:c.2068+15A>T ENSP00000403792.1:n.2068+15A>T
ENST00000542601.6:c.2128+15A>T ENSP00000439156.2:n.2128+15A>T
NM_000095.2:c.2227+15A>T NP_000086.2:n.2227+15A>T
NM_000095.3:c.2227+15A>T MANE Select NP_000086.2:n.2227+15A>T