Canonical Allele Identifier: CA97479100

Gene: SRD5A3

Linked Data

• dbSNP Id: rs939217745
• gnomAD v3: 4-55346226-T-C
• gnomAD v4: 4-55346226-T-C
• MyVariant Identifiers: chr4:g.56212393T>C (hg19) ; chr4:g.55346226T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55346226T>C , CM000666.2:g.55346226T>C	GRCh38
NC_000004.11:g.56212393T>C , CM000666.1:g.56212393T>C	GRCh37
NC_000004.10:g.55907150T>C	NCBI36
NG_028230.1:g.5006T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679836.1:c.-111T>C	ENSP00000506601.1:n.-111T>C
ENST00000264228.8:c.-111T>C	ENSP00000264228.4:n.-111T>C
NM_024592.4:c.-111T>C	NP_078868.1:n.-111T>C