Canonical Allele Identifier: CA2326526620
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787976T= , CM000681.2:g.18787976T= GRCh38
NC_000019.9:g.18898785T= , CM000681.1:g.18898785T= GRCh37
NC_000019.8:g.18759785T= NCBI36
NG_007070.1:g.8330A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.975+236A= MANE Select ENSP00000222271.2:n.975+236A=
ENST00000222271.6:c.975+236A= ENSP00000222271.2:n.975+236A=
ENST00000425807.1:c.816+236A= ENSP00000403792.1:n.816+236A=
ENST00000542601.6:c.876+236A= ENSP00000439156.2:n.876+236A=
NM_000095.2:c.975+236A= NP_000086.2:n.975+236A=
NM_000095.3:c.975+236A= MANE Select NP_000086.2:n.975+236A=
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