Canonical Allele Identifier: CA2326526612
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787964C= , CM000681.2:g.18787964C= GRCh38
NC_000019.9:g.18898773C= , CM000681.1:g.18898773C= GRCh37
NC_000019.8:g.18759773C= NCBI36
NG_007070.1:g.8342G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.975+248G= MANE Select ENSP00000222271.2:n.975+248G=
ENST00000222271.6:c.975+248G= ENSP00000222271.2:n.975+248G=
ENST00000425807.1:c.816+248G= ENSP00000403792.1:n.816+248G=
ENST00000542601.6:c.876+248G= ENSP00000439156.2:n.876+248G=
NM_000095.2:c.975+248G= NP_000086.2:n.975+248G=
NM_000095.3:c.975+248G= MANE Select NP_000086.2:n.975+248G=
Search 100 bp 5'
Search 100 bp 3'