Canonical Allele Identifier: CA506052720
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18896929C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786119C>T , CM000681.2:g.18786119C>T GRCh38
NC_000019.9:g.18896929C>T , CM000681.1:g.18896929C>T GRCh37
NC_000019.8:g.18757929C>T NCBI36
NG_007070.1:g.10186G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1335G>A MANE Select ENSP00000222271.2:p.Arg445=
ENST00000222271.6:c.1335G>A ENSP00000222271.2:p.Arg445=
ENST00000425807.1:c.1176G>A ENSP00000403792.1:p.Arg392=
ENST00000542601.6:c.1236G>A ENSP00000439156.2:p.Arg412=
ENST00000612179.1:n.585G>A
NM_000095.2:c.1335G>A NP_000086.2:p.Arg445=
NM_000095.3:c.1335G>A MANE Select NP_000086.2:p.Arg445=