Canonical Allele Identifier: CA2326526331
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787806A= , CM000681.2:g.18787806A= GRCh38
NC_000019.9:g.18898615A= , CM000681.1:g.18898615A= GRCh37
NC_000019.8:g.18759615A= NCBI36
NG_007070.1:g.8500T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-156T= MANE Select ENSP00000222271.2:n.976-156T=
ENST00000222271.6:c.976-156T= ENSP00000222271.2:n.976-156T=
ENST00000425807.1:c.817-156T= ENSP00000403792.1:n.817-156T=
ENST00000542601.6:c.877-156T= ENSP00000439156.2:n.877-156T=
NM_000095.2:c.976-156T= NP_000086.2:n.976-156T=
NM_000095.3:c.976-156T= MANE Select NP_000086.2:n.976-156T=
Search 100 bp 5'
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