Canonical Allele Identifier: CA404896528
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18900064T>C (hg19) chr19:g.18789255T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789255T>C , CM000681.2:g.18789255T>C GRCh38
NC_000019.9:g.18900064T>C , CM000681.1:g.18900064T>C GRCh37
NC_000019.8:g.18761064T>C NCBI36
NG_007070.1:g.7051A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.433A>G MANE Select ENSP00000222271.2:p.Thr145Ala
ENST00000222271.6:c.433A>G ENSP00000222271.2:p.Thr145Ala
ENST00000425807.1:c.391-363A>G ENSP00000403792.1:n.391-363A>G
ENST00000542601.6:c.334A>G ENSP00000439156.2:p.Thr112Ala
NM_000095.2:c.433A>G NP_000086.2:p.Thr145Ala
NM_000095.3:c.433A>G MANE Select NP_000086.2:p.Thr145Ala
Search 100 bp 5'
Search 100 bp 3'