Canonical Allele Identifier: CA2326526637
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18788006C= , CM000681.2:g.18788006C= GRCh38
NC_000019.9:g.18898815C= , CM000681.1:g.18898815C= GRCh37
NC_000019.8:g.18759815C= NCBI36
NG_007070.1:g.8300G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.975+206G= MANE Select ENSP00000222271.2:n.975+206G=
ENST00000222271.6:c.975+206G= ENSP00000222271.2:n.975+206G=
ENST00000425807.1:c.816+206G= ENSP00000403792.1:n.816+206G=
ENST00000542601.6:c.876+206G= ENSP00000439156.2:n.876+206G=
NM_000095.2:c.975+206G= NP_000086.2:n.975+206G=
NM_000095.3:c.975+206G= MANE Select NP_000086.2:n.975+206G=
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