Canonical Allele Identifier: CA2326525485
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785953C= , CM000681.2:g.18785953C= GRCh38
NC_000019.9:g.18896763C= , CM000681.1:g.18896763C= GRCh37
NC_000019.8:g.18757763C= NCBI36
NG_007070.1:g.10352G=

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1489+12G= MANE Select ENSP00000222271.2:n.1489+12G=
ENST00000222271.6:c.1489+12G= ENSP00000222271.2:n.1489+12G=
ENST00000425807.1:c.1330+12G= ENSP00000403792.1:n.1330+12G=
ENST00000542601.6:c.1390+12G= ENSP00000439156.2:n.1390+12G=
NM_000095.2:c.1489+12G= NP_000086.2:n.1489+12G=
NM_000095.3:c.1489+12G= MANE Select NP_000086.2:n.1489+12G=
Search 100 bp 5'
Search 100 bp 3'