Canonical Allele Identifier: CA555912
Gene: CHD5 HGNC NCBI

Linked Data

dbSNP Id: rs772790386
ExAC: 1:6172219 G / A
gnomAD v2: 1-6172219-G-A
gnomAD v3: 1-6112159-G-A
gnomAD v4: 1-6112159-G-A
COSMIC: COSM4905421 COSM4905422
MyVariant Identifiers: chr1:g.6172219G>A (hg19) chr1:g.6112159G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6112159G>A , CM000663.2:g.6112159G>A GRCh38
NC_000001.10:g.6172219G>A , CM000663.1:g.6172219G>A GRCh37
NC_000001.9:g.6094806G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262450.8:c.5121C>T MANE Select ENSP00000262450.3:p.Ile1707=
ENST00000262450.7:c.5121C>T ENSP00000262450.3:p.Ile1707=
ENST00000377999.5:c.2024C>T ENSP00000367238.2:n.2024C>T
ENST00000462991.5:c.3374C>T
ENST00000496404.1:c.3839C>T ENSP00000433676.1:n.3839C>T
NM_015557.2:c.5121C>T NP_056372.1:p.Ile1707=
NM_015557.3:c.5121C>T MANE Select NP_056372.1:p.Ile1707=
Search 100 bp 5'
Search 100 bp 3'