Canonical Allele Identifier: CA2670662674
Gene: SRD5A3 HGNC NCBI

Linked Data

gnomAD v4: 4-55346329-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346329C>A , CM000666.2:g.55346329C>A GRCh38
NC_000004.11:g.56212496C>A , CM000666.1:g.56212496C>A GRCh37
NC_000004.10:g.55907253C>A NCBI36
NG_028230.1:g.5109C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.-8C>A MANE Select ENSP00000264228.4:n.-8C>A
ENST00000679351.1:c.-8C>A ENSP00000505676.1:n.-8C>A
ENST00000679707.1:c.-8C>A ENSP00000505713.1:n.-8C>A
ENST00000679836.1:c.-8C>A ENSP00000506601.1:n.-8C>A
ENST00000264228.8:c.-8C>A ENSP00000264228.4:n.-8C>A
NM_024592.4:c.-8C>A NP_078868.1:n.-8C>A
XM_005265766.2:c.-8C>A XP_005265823.1:n.-8C>A
XM_005265767.2:c.-8C>A XP_005265824.1:n.-8C>A
XM_005265766.4:c.-8C>A XP_005265823.1:n.-8C>A
XM_005265767.3:c.-8C>A XP_005265824.1:n.-8C>A
NM_024592.5:c.-8C>A MANE Select NP_078868.1:n.-8C>A