Canonical Allele Identifier: CA591408156

Linked Data

dbSNP Id: rs1554785534
gnomAD v2: 10-5140977-G-T
gnomAD v4: 10-5098785-G-T
MyVariant Identifiers: chr10:g.5140977G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098785G>T , CM000672.2:g.5098785G>T GRCh38
NC_000010.10:g.5140977G>T , CM000672.1:g.5140977G>T GRCh37
NC_000010.9:g.5130977G>T NCBI36
NG_047094.1:g.55020G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.370-17G>T (AKR1C3) MANE Select ENSP00000369927.3:n.370-17G>T
ENST00000380554.4:c.370-17G>T (AKR1C3) ENSP00000369927.3:n.370-17G>T
ENST00000407674.5:c.180+33889C>A (AKR1C2) ENSP00000385221.2:n.180+33889C>A
ENST00000434459.6:c.933-8676G>T (AKR1C1) ENSP00000412248.3:n.933-8676G>T
ENST00000439082.7:c.370-17G>T ENSP00000401327.3:n.370-17G>T
ENST00000602997.5:c.301-17G>T (AKR1C3) ENSP00000474188.1:n.301-17G>T
ENST00000605149.5:c.301-17G>T (AKR1C3) ENSP00000474882.1:n.301-17G>T
ENST00000605322.1:n.280-542G>T (AKR1C3)
ENST00000605781.5:n.549-17G>T (AKR1C3)
NM_001253908.1:c.370-17G>T (AKR1C3) NP_001240837.1:n.370-17G>T
NM_003739.5:c.370-17G>T (AKR1C3) NP_003730.4:n.370-17G>T
NM_003739.6:c.370-17G>T (AKR1C3) MANE Select NP_003730.4:n.370-17G>T
NM_001253908.2:c.370-17G>T (AKR1C3) NP_001240837.1:n.370-17G>T