Canonical Allele Identifier: CA796416329
Gene: SRD5A3 HGNC NCBI

Linked Data

dbSNP Id: rs1306670428
gnomAD v3: 4-55346133-G-A
gnomAD v4: 4-55346133-G-A
MyVariant Identifiers: chr4:g.56212300G>A (hg19) chr4:g.55346133G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346133G>A , CM000666.2:g.55346133G>A GRCh38
NC_000004.11:g.56212300G>A , CM000666.1:g.56212300G>A GRCh37
NC_000004.10:g.55907057G>A NCBI36
NG_028230.1:g.4913G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.8:c.-204G>A ENSP00000264228.4:n.-204G>A
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