Canonical Allele Identifier: CA555913
Gene: CHD5 HGNC NCBI

Linked Data

dbSNP Id: rs375091569
ExAC: 1:6172234 C / T
gnomAD v2: 1-6172234-C-T
gnomAD v3: 1-6112174-C-T
gnomAD v4: 1-6112174-C-T
MyVariant Identifiers: chr1:g.6172234C>T (hg19) chr1:g.6112174C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6112174C>T , CM000663.2:g.6112174C>T GRCh38
NC_000001.10:g.6172234C>T , CM000663.1:g.6172234C>T GRCh37
NC_000001.9:g.6094821C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262450.8:c.5106G>A MANE Select ENSP00000262450.3:p.Lys1702=
ENST00000262450.7:c.5106G>A ENSP00000262450.3:p.Lys1702=
ENST00000377999.5:c.2009G>A ENSP00000367238.2:n.2009G>A
ENST00000462991.5:c.3359G>A
ENST00000496404.1:c.3824G>A ENSP00000433676.1:n.3824G>A
NM_015557.2:c.5106G>A NP_056372.1:p.Lys1702=
NM_015557.3:c.5106G>A MANE Select NP_056372.1:p.Lys1702=
Search 100 bp 5'
Search 100 bp 3'