Canonical Allele Identifier: CA404879358
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18785086G>C , CM000681.2:g.18785086G>C GRCh38
NC_000019.9:g.18895896G>C , CM000681.1:g.18895896G>C GRCh37
NC_000019.8:g.18756896G>C NCBI36
NG_007070.1:g.11219C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1724C>G MANE Select ENSP00000222271.2:p.Thr575Ser
ENST00000222271.6:c.1724C>G ENSP00000222271.2:p.Thr575Ser
ENST00000425807.1:c.1565C>G ENSP00000403792.1:p.Thr522Ser
ENST00000542601.6:c.1625C>G ENSP00000439156.2:p.Thr542Ser
NM_000095.2:c.1724C>G NP_000086.2:p.Thr575Ser
NM_000095.3:c.1724C>G MANE Select NP_000086.2:p.Thr575Ser