Canonical Allele Identifier: CA2670662194
Gene: SRD5A3 HGNC NCBI

Linked Data

dbSNP Id: rs2109455865
gnomAD v4: 4-55346258-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346258G>T , CM000666.2:g.55346258G>T GRCh38
NC_000004.11:g.56212425G>T , CM000666.1:g.56212425G>T GRCh37
NC_000004.10:g.55907182G>T NCBI36
NG_028230.1:g.5038G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.-79G>T MANE Select ENSP00000264228.4:n.-79G>T
ENST00000679707.1:c.-79G>T ENSP00000505713.1:n.-79G>T
ENST00000679836.1:c.-79G>T ENSP00000506601.1:n.-79G>T
ENST00000264228.8:c.-79G>T ENSP00000264228.4:n.-79G>T
NM_024592.4:c.-79G>T NP_078868.1:n.-79G>T
XM_005265766.2:c.-79G>T XP_005265823.1:n.-79G>T
XM_005265767.2:c.-79G>T XP_005265824.1:n.-79G>T
XM_005265766.4:c.-79G>T XP_005265823.1:n.-79G>T
XM_005265767.3:c.-79G>T XP_005265824.1:n.-79G>T
NM_024592.5:c.-79G>T MANE Select NP_078868.1:n.-79G>T