Canonical Allele Identifier: CA2326523970
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18783037G= , CM000681.2:g.18783037G= GRCh38
NC_000019.9:g.18893847G= , CM000681.1:g.18893847G= GRCh37
NC_000019.8:g.18754847G= NCBI36
NG_007070.1:g.13268C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.2227+17C= MANE Select ENSP00000222271.2:n.2227+17C=
ENST00000222271.6:c.2227+17C= ENSP00000222271.2:n.2227+17C=
ENST00000425807.1:c.2068+17C= ENSP00000403792.1:n.2068+17C=
ENST00000542601.6:c.2128+17C= ENSP00000439156.2:n.2128+17C=
NM_000095.2:c.2227+17C= NP_000086.2:n.2227+17C=
NM_000095.3:c.2227+17C= MANE Select NP_000086.2:n.2227+17C=