Canonical Allele Identifier: CA551566762
Gene: SRD5A3 HGNC NCBI

Linked Data

dbSNP Id: rs1319002124
gnomAD v2: 4-56212398-G-T
gnomAD v3: 4-55346231-G-T
gnomAD v4: 4-55346231-G-T
MyVariant Identifiers: chr4:g.56212398G>T (hg19) chr4:g.55346231G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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