Canonical Allele Identifier: CA404896478
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18900052A>C (hg19) chr19:g.18789243A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789243A>C , CM000681.2:g.18789243A>C GRCh38
NC_000019.9:g.18900052A>C , CM000681.1:g.18900052A>C GRCh37
NC_000019.8:g.18761052A>C NCBI36
NG_007070.1:g.7063T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.445T>G MANE Select ENSP00000222271.2:p.Phe149Val
ENST00000222271.6:c.445T>G ENSP00000222271.2:p.Phe149Val
ENST00000425807.1:c.391-351T>G ENSP00000403792.1:n.391-351T>G
ENST00000542601.6:c.346T>G ENSP00000439156.2:p.Phe116Val
NM_000095.2:c.445T>G NP_000086.2:p.Phe149Val
NM_000095.3:c.445T>G MANE Select NP_000086.2:p.Phe149Val
Search 100 bp 5'
Search 100 bp 3'