Canonical Allele Identifier: CA97479102
Gene: SRD5A3 HGNC NCBI

Linked Data

dbSNP Id: rs905256180
gnomAD v3: 4-55346230-C-G
gnomAD v4: 4-55346230-C-G
MyVariant Identifiers: chr4:g.56212397C>G (hg19) chr4:g.55346230C>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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