Canonical Allele Identifier: CA467990793

Linked Data

dbSNP Id: rs369662312
gnomAD v2: 10-5141050-G-C
MyVariant Identifiers: chr10:g.5141050G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098858G>C , CM000672.2:g.5098858G>C GRCh38
NC_000010.10:g.5141050G>C , CM000672.1:g.5141050G>C GRCh37
NC_000010.9:g.5131050G>C NCBI36
NG_047094.1:g.55093G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000380554.5:c.426G>C (AKR1C3) MANE Select ENSP00000369927.3:p.Val142=
ENST00000380554.4:c.426G>C (AKR1C3) ENSP00000369927.3:p.Val142=
ENST00000407674.5:c.180+33816C>G (AKR1C2) ENSP00000385221.2:n.180+33816C>G
ENST00000434459.6:c.933-8603G>C (AKR1C1) ENSP00000412248.3:n.933-8603G>C
ENST00000439082.7:c.426G>C ENSP00000401327.3:p.Val142=
ENST00000602997.5:c.357G>C (AKR1C3) ENSP00000474188.1:p.Val119=
ENST00000605149.5:c.357G>C (AKR1C3) ENSP00000474882.1:p.Val119=
ENST00000605322.1:n.280-469G>C (AKR1C3)
ENST00000605781.5:n.605G>C (AKR1C3)
NM_001253908.1:c.426G>C (AKR1C3) NP_001240837.1:p.Val142=
NM_003739.5:c.426G>C (AKR1C3) NP_003730.4:p.Val142=
NM_003739.6:c.426G>C (AKR1C3) MANE Select NP_003730.4:p.Val142=
NM_001253908.2:c.426G>C (AKR1C3) NP_001240837.1:p.Val142=