Canonical Allele Identifier: CA796416433
Gene: SRD5A3 HGNC NCBI

Linked Data

dbSNP Id: rs1319002124
gnomAD v4: 4-55346231-G-C
MyVariant Identifiers: chr4:g.56212398G>C (hg19) chr4:g.55346231G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346231G>C , CM000666.2:g.55346231G>C GRCh38
NC_000004.11:g.56212398G>C , CM000666.1:g.56212398G>C GRCh37
NC_000004.10:g.55907155G>C NCBI36
NG_028230.1:g.5011G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000679707.1:c.-106G>C ENSP00000505713.1:n.-106G>C
ENST00000679836.1:c.-106G>C ENSP00000506601.1:n.-106G>C
ENST00000264228.8:c.-106G>C ENSP00000264228.4:n.-106G>C
NM_024592.4:c.-106G>C NP_078868.1:n.-106G>C
XM_005265767.3:c.-106G>C XP_005265824.1:n.-106G>C
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