Canonical Allele Identifier: CA5390581

Linked Data

dbSNP Id: rs782342902
gnomAD v2: 10-5141108-C-G
gnomAD v3: 10-5098916-C-G
gnomAD v4: 10-5098916-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098916C>G , CM000672.2:g.5098916C>G GRCh38
NC_000010.10:g.5141108C>G , CM000672.1:g.5141108C>G GRCh37
NC_000010.9:g.5131108C>G NCBI36
NG_047094.1:g.55151C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+37C>G (AKR1C3) MANE Select ENSP00000369927.3:n.447+37C>G
ENST00000380554.4:c.447+37C>G (AKR1C3) ENSP00000369927.3:n.447+37C>G
ENST00000407674.5:c.180+33758G>C (AKR1C2) ENSP00000385221.2:n.180+33758G>C
ENST00000434459.6:c.933-8545C>G (AKR1C1) ENSP00000412248.3:n.933-8545C>G
ENST00000439082.7:c.447+37C>G ENSP00000401327.3:n.447+37C>G
ENST00000602997.5:c.378+37C>G (AKR1C3) ENSP00000474188.1:n.378+37C>G
ENST00000605149.5:c.378+37C>G (AKR1C3) ENSP00000474882.1:n.378+37C>G
ENST00000605322.1:n.280-411C>G (AKR1C3)
ENST00000605781.5:n.626+37C>G (AKR1C3)
NM_001253908.1:c.447+37C>G (AKR1C3) NP_001240837.1:n.447+37C>G
NM_003739.5:c.447+37C>G (AKR1C3) NP_003730.4:n.447+37C>G
NM_003739.6:c.447+37C>G (AKR1C3) MANE Select NP_003730.4:n.447+37C>G
NM_001253908.2:c.447+37C>G (AKR1C3) NP_001240837.1:n.447+37C>G