Canonical Allele Identifier: CA2326526592
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787925G= , CM000681.2:g.18787925G= GRCh38
NC_000019.9:g.18898734G= , CM000681.1:g.18898734G= GRCh37
NC_000019.8:g.18759734G= NCBI36
NG_007070.1:g.8381C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-275C= MANE Select ENSP00000222271.2:n.976-275C=
ENST00000222271.6:c.976-275C= ENSP00000222271.2:n.976-275C=
ENST00000425807.1:c.817-275C= ENSP00000403792.1:n.817-275C=
ENST00000542601.6:c.877-275C= ENSP00000439156.2:n.877-275C=
NM_000095.2:c.976-275C= NP_000086.2:n.976-275C=
NM_000095.3:c.976-275C= MANE Select NP_000086.2:n.976-275C=
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