Canonical Allele Identifier: CA404896530
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18900065G>T (hg19) chr19:g.18789256G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789256G>T , CM000681.2:g.18789256G>T GRCh38
NC_000019.9:g.18900065G>T , CM000681.1:g.18900065G>T GRCh37
NC_000019.8:g.18761065G>T NCBI36
NG_007070.1:g.7050C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.432C>A MANE Select ENSP00000222271.2:p.Asn144Lys
ENST00000222271.6:c.432C>A ENSP00000222271.2:p.Asn144Lys
ENST00000425807.1:c.391-364C>A ENSP00000403792.1:n.391-364C>A
ENST00000542601.6:c.333C>A ENSP00000439156.2:p.Asn111Lys
NM_000095.2:c.432C>A NP_000086.2:p.Asn144Lys
NM_000095.3:c.432C>A MANE Select NP_000086.2:p.Asn144Lys
Search 100 bp 5'
Search 100 bp 3'