Canonical Allele Identifier: CA2326527293
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789318G= , CM000681.2:g.18789318G= GRCh38
NC_000019.9:g.18900127G= , CM000681.1:g.18900127G= GRCh37
NC_000019.8:g.18761127G= NCBI36
NG_007070.1:g.6988C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.391-21C= MANE Select ENSP00000222271.2:n.391-21C=
ENST00000222271.6:c.391-21C= ENSP00000222271.2:n.391-21C=
ENST00000425807.1:c.391-426C= ENSP00000403792.1:n.391-426C=
ENST00000542601.6:c.292-21C= ENSP00000439156.2:n.292-21C=
NM_000095.2:c.391-21C= NP_000086.2:n.391-21C=
NM_000095.3:c.391-21C= MANE Select NP_000086.2:n.391-21C=
Search 100 bp 5'
Search 100 bp 3'