Canonical Allele Identifier: CA666181129

Linked Data

dbSNP Id: rs1334328744
gnomAD v3: 10-5098763-T-G
gnomAD v4: 10-5098763-T-G
MyVariant Identifiers: chr10:g.5098763T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098763T>G , CM000672.2:g.5098763T>G GRCh38
NC_000010.10:g.5140955T>G , CM000672.1:g.5140955T>G GRCh37
NC_000010.9:g.5130955T>G NCBI36
NG_047094.1:g.54998T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380554.5:c.370-39T>G (AKR1C3) MANE Select ENSP00000369927.3:n.370-39T>G
ENST00000380554.4:c.370-39T>G (AKR1C3) ENSP00000369927.3:n.370-39T>G
ENST00000407674.5:c.180+33911A>C (AKR1C2) ENSP00000385221.2:n.180+33911A>C
ENST00000434459.6:c.933-8698T>G (AKR1C1) ENSP00000412248.3:n.933-8698T>G
ENST00000439082.7:c.370-39T>G ENSP00000401327.3:n.370-39T>G
ENST00000602997.5:c.301-39T>G (AKR1C3) ENSP00000474188.1:n.301-39T>G
ENST00000605149.5:c.301-39T>G (AKR1C3) ENSP00000474882.1:n.301-39T>G
ENST00000605322.1:n.280-564T>G (AKR1C3)
ENST00000605781.5:n.549-39T>G (AKR1C3)
NM_001253908.1:c.370-39T>G (AKR1C3) NP_001240837.1:n.370-39T>G
NM_003739.5:c.370-39T>G (AKR1C3) NP_003730.4:n.370-39T>G
NM_003739.6:c.370-39T>G (AKR1C3) MANE Select NP_003730.4:n.370-39T>G
NM_001253908.2:c.370-39T>G (AKR1C3) NP_001240837.1:n.370-39T>G