Canonical Allele Identifier: CA9316545
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs754522846

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787527G>A , CM000681.2:g.18787527G>A GRCh38
NC_000019.9:g.18898336G>A , CM000681.1:g.18898336G>A GRCh37
NC_000019.8:g.18759336G>A NCBI36
NG_007070.1:g.8779C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1099C>T MANE Select ENSP00000222271.2:p.Arg367Trp
ENST00000222271.6:c.1099C>T ENSP00000222271.2:p.Arg367Trp
ENST00000425807.1:c.940C>T ENSP00000403792.1:p.Arg314Trp
ENST00000542601.6:c.1000C>T ENSP00000439156.2:p.Arg334Trp
NM_000095.2:c.1099C>T NP_000086.2:p.Arg367Trp
NM_000095.3:c.1099C>T MANE Select NP_000086.2:p.Arg367Trp