Canonical Allele Identifier: CA97479101
Gene: SRD5A3 HGNC NCBI

Linked Data

dbSNP Id: rs905256180
gnomAD v3: 4-55346230-C-A
gnomAD v4: 4-55346230-C-A
MyVariant Identifiers: chr4:g.55346230C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346230C>A , CM000666.2:g.55346230C>A GRCh38
NC_000004.11:g.56212397C>A , CM000666.1:g.56212397C>A GRCh37
NC_000004.10:g.55907154C>A NCBI36
NG_028230.1:g.5010C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679707.1:c.-107C>A ENSP00000505713.1:n.-107C>A
ENST00000679836.1:c.-107C>A ENSP00000506601.1:n.-107C>A
ENST00000264228.8:c.-107C>A ENSP00000264228.4:n.-107C>A
NM_024592.4:c.-107C>A NP_078868.1:n.-107C>A
XM_005265767.3:c.-107C>A XP_005265824.1:n.-107C>A
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