Canonical Allele Identifier: CA97479081
Gene: SRD5A3 HGNC NCBI

Linked Data

dbSNP Id: rs952951374
gnomAD v3: 4-55346152-G-C
gnomAD v4: 4-55346152-G-C
MyVariant Identifiers: chr4:g.56212319G>C (hg19) chr4:g.55346152G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346152G>C , CM000666.2:g.55346152G>C GRCh38
NC_000004.11:g.56212319G>C , CM000666.1:g.56212319G>C GRCh37
NC_000004.10:g.55907076G>C NCBI36
NG_028230.1:g.4932G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.8:c.-185G>C ENSP00000264228.4:n.-185G>C
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