Canonical Allele Identifier: CA2326526429
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787856T= , CM000681.2:g.18787856T= GRCh38
NC_000019.9:g.18898665T= , CM000681.1:g.18898665T= GRCh37
NC_000019.8:g.18759665T= NCBI36
NG_007070.1:g.8450A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-206A= MANE Select ENSP00000222271.2:n.976-206A=
ENST00000222271.6:c.976-206A= ENSP00000222271.2:n.976-206A=
ENST00000425807.1:c.817-206A= ENSP00000403792.1:n.817-206A=
ENST00000542601.6:c.877-206A= ENSP00000439156.2:n.877-206A=
NM_000095.2:c.976-206A= NP_000086.2:n.976-206A=
NM_000095.3:c.976-206A= MANE Select NP_000086.2:n.976-206A=
Search 100 bp 5'
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