Canonical Allele Identifier: CA306255509
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs754289056

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786181C>T , CM000681.2:g.18786181C>T GRCh38
NC_000019.9:g.18896991C>T , CM000681.1:g.18896991C>T GRCh37
NC_000019.8:g.18757991C>T NCBI36
NG_007070.1:g.10124G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1308-35G>A MANE Select ENSP00000222271.2:n.1308-35G>A
ENST00000222271.6:c.1308-35G>A ENSP00000222271.2:n.1308-35G>A
ENST00000425807.1:c.1149-35G>A ENSP00000403792.1:n.1149-35G>A
ENST00000542601.6:c.1209-35G>A ENSP00000439156.2:n.1209-35G>A
ENST00000612179.1:n.558-35G>A
NM_000095.2:c.1308-35G>A NP_000086.2:n.1308-35G>A
NM_000095.3:c.1308-35G>A MANE Select NP_000086.2:n.1308-35G>A