Canonical Allele Identifier: CA666181405

Linked Data

dbSNP Id: rs1468455841
gnomAD v3: 10-5098983-A-C
gnomAD v4: 10-5098983-A-C
MyVariant Identifiers: chr10:g.5098983A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098983A>C , CM000672.2:g.5098983A>C GRCh38
NC_000010.10:g.5141175A>C , CM000672.1:g.5141175A>C GRCh37
NC_000010.9:g.5131175A>C NCBI36
NG_047094.1:g.55218A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000380554.5:c.447+104A>C (AKR1C3) MANE Select ENSP00000369927.3:n.447+104A>C
ENST00000380554.4:c.447+104A>C (AKR1C3) ENSP00000369927.3:n.447+104A>C
ENST00000407674.5:c.180+33691T>G (AKR1C2) ENSP00000385221.2:n.180+33691T>G
ENST00000434459.6:c.933-8478A>C (AKR1C1) ENSP00000412248.3:n.933-8478A>C
ENST00000439082.7:c.447+104A>C ENSP00000401327.3:n.447+104A>C
ENST00000602997.5:c.378+104A>C (AKR1C3) ENSP00000474188.1:n.378+104A>C
ENST00000605149.5:c.378+104A>C (AKR1C3) ENSP00000474882.1:n.378+104A>C
ENST00000605322.1:n.280-344A>C (AKR1C3)
ENST00000605781.5:n.626+104A>C (AKR1C3)
NM_001253908.1:c.447+104A>C (AKR1C3) NP_001240837.1:n.447+104A>C
NM_003739.5:c.447+104A>C (AKR1C3) NP_003730.4:n.447+104A>C
NM_003739.6:c.447+104A>C (AKR1C3) MANE Select NP_003730.4:n.447+104A>C
NM_001253908.2:c.447+104A>C (AKR1C3) NP_001240837.1:n.447+104A>C