Canonical Allele Identifier: CA2326524870
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18784909C= , CM000681.2:g.18784909C= GRCh38
NC_000019.9:g.18895719C= , CM000681.1:g.18895719C= GRCh37
NC_000019.8:g.18756719C= NCBI36
NG_007070.1:g.11396G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1901G= MANE Select ENSP00000222271.2:p.Gly634=
ENST00000222271.6:c.1901G= ENSP00000222271.2:p.Gly634=
ENST00000425807.1:c.1742G= ENSP00000403792.1:p.Gly581=
ENST00000542601.6:c.1802G= ENSP00000439156.2:p.Gly601=
NM_000095.2:c.1901G= NP_000086.2:p.Gly634=
NM_000095.3:c.1901G= MANE Select NP_000086.2:p.Gly634=