Canonical Allele Identifier: CA404890329
Gene: COMP HGNC NCBI

Linked Data

gnomAD v3: 19-18787635-C-T
gnomAD v4: 19-18787635-C-T
MyVariant Identifiers: chr19:g.18898444C>T (hg19) chr19:g.18787635C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787635C>T , CM000681.2:g.18787635C>T GRCh38
NC_000019.9:g.18898444C>T , CM000681.1:g.18898444C>T GRCh37
NC_000019.8:g.18759444C>T NCBI36
NG_007070.1:g.8671G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.991G>A MANE Select ENSP00000222271.2:p.Val331Met
ENST00000222271.6:c.991G>A ENSP00000222271.2:p.Val331Met
ENST00000425807.1:c.832G>A ENSP00000403792.1:p.Val278Met
ENST00000542601.6:c.892G>A ENSP00000439156.2:p.Val298Met
NM_000095.2:c.991G>A NP_000086.2:p.Val331Met
NM_000095.3:c.991G>A MANE Select NP_000086.2:p.Val331Met
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