Canonical Allele Identifier: CA306255348
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs780461514
gnomAD v3: 19-18786066-C-A
gnomAD v4: 19-18786066-C-A
MyVariant Identifiers: chr19:g.18896876C>A (hg19) chr19:g.18786066C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786066C>A , CM000681.2:g.18786066C>A GRCh38
NC_000019.9:g.18896876C>A , CM000681.1:g.18896876C>A GRCh37
NC_000019.8:g.18757876C>A NCBI36
NG_007070.1:g.10239G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1388G>T MANE Select ENSP00000222271.2:p.Gly463Val
ENST00000222271.6:c.1388G>T ENSP00000222271.2:p.Gly463Val
ENST00000425807.1:c.1229G>T ENSP00000403792.1:p.Gly410Val
ENST00000542601.6:c.1289G>T ENSP00000439156.2:p.Gly430Val
NM_000095.2:c.1388G>T NP_000086.2:p.Gly463Val
NM_000095.3:c.1388G>T MANE Select NP_000086.2:p.Gly463Val
Search 100 bp 5'
Search 100 bp 3'