Canonical Allele Identifier: CA2326525623
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786199C= , CM000681.2:g.18786199C= GRCh38
NC_000019.9:g.18897009C= , CM000681.1:g.18897009C= GRCh37
NC_000019.8:g.18758009C= NCBI36
NG_007070.1:g.10106G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1307+40G= MANE Select ENSP00000222271.2:n.1307+40G=
ENST00000222271.6:c.1307+40G= ENSP00000222271.2:n.1307+40G=
ENST00000425807.1:c.1148+40G= ENSP00000403792.1:n.1148+40G=
ENST00000542601.6:c.1208+40G= ENSP00000439156.2:n.1208+40G=
ENST00000612179.1:n.557+40G=
NM_000095.2:c.1307+40G= NP_000086.2:n.1307+40G=
NM_000095.3:c.1307+40G= MANE Select NP_000086.2:n.1307+40G=
Search 100 bp 5'
Search 100 bp 3'