Canonical Allele Identifier: CA404888628
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1285692110

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787604T>C , CM000681.2:g.18787604T>C GRCh38
NC_000019.9:g.18898413T>C , CM000681.1:g.18898413T>C GRCh37
NC_000019.8:g.18759413T>C NCBI36
NG_007070.1:g.8702A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1022A>G MANE Select ENSP00000222271.2:p.Glu341Gly
ENST00000222271.6:c.1022A>G ENSP00000222271.2:p.Glu341Gly
ENST00000425807.1:c.863A>G ENSP00000403792.1:p.Glu288Gly
ENST00000542601.6:c.923A>G ENSP00000439156.2:p.Glu308Gly
NM_000095.2:c.1022A>G NP_000086.2:p.Glu341Gly
NM_000095.3:c.1022A>G MANE Select NP_000086.2:p.Glu341Gly