Canonical Allele Identifier: CA2670662080
Gene: SRD5A3 HGNC NCBI

Linked Data

gnomAD v4: 4-55346242-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346242A>C , CM000666.2:g.55346242A>C GRCh38
NC_000004.11:g.56212409A>C , CM000666.1:g.56212409A>C GRCh37
NC_000004.10:g.55907166A>C NCBI36
NG_028230.1:g.5022A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.-95A>C MANE Select ENSP00000264228.4:n.-95A>C
ENST00000679707.1:c.-95A>C ENSP00000505713.1:n.-95A>C
ENST00000679836.1:c.-95A>C ENSP00000506601.1:n.-95A>C
ENST00000264228.8:c.-95A>C ENSP00000264228.4:n.-95A>C
NM_024592.4:c.-95A>C NP_078868.1:n.-95A>C
XM_005265766.2:c.-95A>C XP_005265823.1:n.-95A>C
XM_005265766.4:c.-95A>C XP_005265823.1:n.-95A>C
XM_005265767.3:c.-95A>C XP_005265824.1:n.-95A>C
NM_024592.5:c.-95A>C MANE Select NP_078868.1:n.-95A>C
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