Canonical Allele Identifier: CA506117460
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18896872C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786062C>T , CM000681.2:g.18786062C>T GRCh38
NC_000019.9:g.18896872C>T , CM000681.1:g.18896872C>T GRCh37
NC_000019.8:g.18757872C>T NCBI36
NG_007070.1:g.10243G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1392G>A MANE Select ENSP00000222271.2:p.Gln464=
ENST00000222271.6:c.1392G>A ENSP00000222271.2:p.Gln464=
ENST00000425807.1:c.1233G>A ENSP00000403792.1:p.Gln411=
ENST00000542601.6:c.1293G>A ENSP00000439156.2:p.Gln431=
NM_000095.2:c.1392G>A NP_000086.2:p.Gln464=
NM_000095.3:c.1392G>A MANE Select NP_000086.2:p.Gln464=