Canonical Allele Identifier: CA2326526509
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787873T= , CM000681.2:g.18787873T= GRCh38
NC_000019.9:g.18898682T= , CM000681.1:g.18898682T= GRCh37
NC_000019.8:g.18759682T= NCBI36
NG_007070.1:g.8433A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-223A= MANE Select ENSP00000222271.2:n.976-223A=
ENST00000222271.6:c.976-223A= ENSP00000222271.2:n.976-223A=
ENST00000425807.1:c.817-223A= ENSP00000403792.1:n.817-223A=
ENST00000542601.6:c.877-223A= ENSP00000439156.2:n.877-223A=
NM_000095.2:c.976-223A= NP_000086.2:n.976-223A=
NM_000095.3:c.976-223A= MANE Select NP_000086.2:n.976-223A=
Search 100 bp 5'
Search 100 bp 3'