Canonical Allele Identifier: CA2583622636
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787663G>T , CM000681.2:g.18787663G>T GRCh38
NC_000019.9:g.18898472G>T , CM000681.1:g.18898472G>T GRCh37
NC_000019.8:g.18759472G>T NCBI36
NG_007070.1:g.8643C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-13C>A MANE Select ENSP00000222271.2:n.976-13C>A
ENST00000222271.6:c.976-13C>A ENSP00000222271.2:n.976-13C>A
ENST00000425807.1:c.817-13C>A ENSP00000403792.1:n.817-13C>A
ENST00000542601.6:c.877-13C>A ENSP00000439156.2:n.877-13C>A
NM_000095.2:c.976-13C>A NP_000086.2:n.976-13C>A
NM_000095.3:c.976-13C>A MANE Select NP_000086.2:n.976-13C>A