Canonical Allele Identifier: CA2326526464
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787522G= , CM000681.2:g.18787522G= GRCh38
NC_000019.9:g.18898331G= , CM000681.1:g.18898331G= GRCh37
NC_000019.8:g.18759331G= NCBI36
NG_007070.1:g.8784C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1104C= MANE Select ENSP00000222271.2:p.Gly368=
ENST00000222271.6:c.1104C= ENSP00000222271.2:p.Gly368=
ENST00000425807.1:c.945C= ENSP00000403792.1:p.Gly315=
ENST00000542601.6:c.1005C= ENSP00000439156.2:p.Gly335=
NM_000095.2:c.1104C= NP_000086.2:p.Gly368=
NM_000095.3:c.1104C= MANE Select NP_000086.2:p.Gly368=