Canonical Allele Identifier: CA404887811
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787511T>C , CM000681.2:g.18787511T>C GRCh38
NC_000019.9:g.18898320T>C , CM000681.1:g.18898320T>C GRCh37
NC_000019.8:g.18759320T>C NCBI36
NG_007070.1:g.8795A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1115A>G MANE Select ENSP00000222271.2:p.Asp372Gly
ENST00000222271.6:c.1115A>G ENSP00000222271.2:p.Asp372Gly
ENST00000425807.1:c.956A>G ENSP00000403792.1:p.Asp319Gly
ENST00000542601.6:c.1016A>G ENSP00000439156.2:p.Asp339Gly
NM_000095.2:c.1115A>G NP_000086.2:p.Asp372Gly
NM_000095.3:c.1115A>G MANE Select NP_000086.2:p.Asp372Gly