Canonical Allele Identifier: CA2326524865
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18784885G= , CM000681.2:g.18784885G= GRCh38
NC_000019.9:g.18895695G= , CM000681.1:g.18895695G= GRCh37
NC_000019.8:g.18756695G= NCBI36
NG_007070.1:g.11420C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1914+11C= MANE Select ENSP00000222271.2:n.1914+11C=
ENST00000222271.6:c.1914+11C= ENSP00000222271.2:n.1914+11C=
ENST00000425807.1:c.1755+11C= ENSP00000403792.1:n.1755+11C=
ENST00000542601.6:c.1815+11C= ENSP00000439156.2:n.1815+11C=
NM_000095.2:c.1914+11C= NP_000086.2:n.1914+11C=
NM_000095.3:c.1914+11C= MANE Select NP_000086.2:n.1914+11C=
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