Canonical Allele Identifier: CA156197
Gene: AKR1C4 HGNC NCBI

Linked Data

ClinVar Variation Id: 132789
ClinVar RCV Id: RCV000119258 RCV000891835
dbSNP Id: rs201441444
ExAC: 10:5247806 T / G
gnomAD v2: 10-5247806-T-G
gnomAD v3: 10-5205843-T-G
gnomAD v4: 10-5205843-T-G
MyVariant Identifiers: chr10:g.5247806T>G (hg19) chr10:g.5205843T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5205843T>G , CM000672.2:g.5205843T>G GRCh38
NC_000010.10:g.5247806T>G , CM000672.1:g.5247806T>G GRCh37
NC_000010.9:g.5237806T>G NCBI36
NG_031872.1:g.14009T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263126.3:c.447+9T>G MANE Select ENSP00000263126.1:n.447+9T>G
ENST00000263126.2:c.447+9T>G ENSP00000263126.1:n.447+9T>G
ENST00000380448.5:c.447+9T>G ENSP00000369814.1:n.447+9T>G
NM_001818.3:c.447+9T>G NP_001809.3:n.447+9T>G
XM_011519303.1:c.456T>G XP_011517605.1:p.Ala152=
NM_001818.4:c.447+9T>G NP_001809.3:n.447+9T>G
NM_001818.5:c.447+9T>G MANE Select NP_001809.4:n.447+9T>G
Search 100 bp 5'
Search 100 bp 3'