Canonical Allele Identifier: CA16378189
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5093956A>G , CM000672.2:g.5093956A>G GRCh38
NC_000010.10:g.5136148A>G , CM000672.1:g.5136148A>G GRCh37
NC_000010.9:g.5126148A>G NCBI36
NG_047094.1:g.50191A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.4:c.-489A>G (AKR1C3) ENSP00000369927.3:n.-489A>G
ENST00000407674.5:c.180+38718T>C (AKR1C2) ENSP00000385221.2:n.180+38718T>C
ENST00000434459.6:c.933-13505A>G (AKR1C1) ENSP00000412248.3:n.933-13505A>G
ENST00000439082.7:c.85-2454A>G ENSP00000401327.3:n.85-2454A>G
ENST00000470862.6:n.729-2454A>G (AKR1C3)
ENST00000480822.5:n.524-2454A>G (AKR1C3)
ENST00000602997.5:c.16-2454A>G (AKR1C3) ENSP00000474188.1:n.16-2454A>G
ENST00000605149.5:c.16-2454A>G (AKR1C3) ENSP00000474882.1:n.16-2454A>G
ENST00000605781.5:n.264-2454A>G (AKR1C3)
NM_001253908.1:c.85-2454A>G (AKR1C3) NP_001240837.1:n.85-2454A>G
NM_001253908.2:c.85-2454A>G (AKR1C3) NP_001240837.1:n.85-2454A>G