Canonical Allele Identifier: CA551566745
Gene: SRD5A3 HGNC NCBI

Linked Data

dbSNP Id: rs1449814932
gnomAD v2: 4-56212295-C-A
gnomAD v3: 4-55346128-C-A
gnomAD v4: 4-55346128-C-A
MyVariant Identifiers: chr4:g.56212295C>A (hg19) chr4:g.55346128C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346128C>A , CM000666.2:g.55346128C>A GRCh38
NC_000004.11:g.56212295C>A , CM000666.1:g.56212295C>A GRCh37
NC_000004.10:g.55907052C>A NCBI36
NG_028230.1:g.4908C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.8:c.-209C>A ENSP00000264228.4:n.-209C>A
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