Canonical Allele Identifier: CA17140221
Gene: CHD5 HGNC NCBI

Linked Data

dbSNP Id: rs150855676
gnomAD v4: 1-6112171-G-A
COSMIC: COSM107121
MyVariant Identifiers: chr1:g.6172231G>A (hg19) chr1:g.6112171G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6112171G>A , CM000663.2:g.6112171G>A GRCh38
NC_000001.10:g.6172231G>A , CM000663.1:g.6172231G>A GRCh37
NC_000001.9:g.6094818G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262450.8:c.5109C>T MANE Select ENSP00000262450.3:p.Phe1703=
ENST00000262450.7:c.5109C>T ENSP00000262450.3:p.Phe1703=
ENST00000377999.5:c.2012C>T ENSP00000367238.2:n.2012C>T
ENST00000462991.5:c.3362C>T
ENST00000496404.1:c.3827C>T ENSP00000433676.1:n.3827C>T
NM_015557.2:c.5109C>T NP_056372.1:p.Phe1703=
NM_015557.3:c.5109C>T MANE Select NP_056372.1:p.Phe1703=
Search 100 bp 5'
Search 100 bp 3'