Canonical Allele Identifier: CA17140237
Gene: CHD5 HGNC NCBI

Linked Data

dbSNP Id: rs202017595
gnomAD v2: 1-6172236-T-G
gnomAD v3: 1-6112176-T-G
gnomAD v4: 1-6112176-T-G
MyVariant Identifiers: chr1:g.6172236T>G (hg19) chr1:g.6112176T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6112176T>G , CM000663.2:g.6112176T>G GRCh38
NC_000001.10:g.6172236T>G , CM000663.1:g.6172236T>G GRCh37
NC_000001.9:g.6094823T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262450.8:c.5104A>C MANE Select ENSP00000262450.3:p.Lys1702Gln
ENST00000262450.7:c.5104A>C ENSP00000262450.3:p.Lys1702Gln
ENST00000377999.5:c.2007A>C ENSP00000367238.2:n.2007A>C
ENST00000462991.5:c.3357A>C
ENST00000496404.1:c.3822A>C ENSP00000433676.1:n.3822A>C
NM_015557.2:c.5104A>C NP_056372.1:p.Lys1702Gln
NM_015557.3:c.5104A>C MANE Select NP_056372.1:p.Lys1702Gln
Search 100 bp 5'
Search 100 bp 3'