Canonical Allele Identifier: CA404896522
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789254G>C , CM000681.2:g.18789254G>C GRCh38
NC_000019.9:g.18900063G>C , CM000681.1:g.18900063G>C GRCh37
NC_000019.8:g.18761063G>C NCBI36
NG_007070.1:g.7052C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.434C>G MANE Select ENSP00000222271.2:p.Thr145Ser
ENST00000222271.6:c.434C>G ENSP00000222271.2:p.Thr145Ser
ENST00000425807.1:c.391-362C>G ENSP00000403792.1:n.391-362C>G
ENST00000542601.6:c.335C>G ENSP00000439156.2:p.Thr112Ser
NM_000095.2:c.434C>G NP_000086.2:p.Thr145Ser
NM_000095.3:c.434C>G MANE Select NP_000086.2:p.Thr145Ser