Canonical Allele Identifier: CA97479118

Gene: SRD5A3

Linked Data

• dbSNP Id: rs925486509
• gnomAD v3: 4-55346332-G-C
• gnomAD v4: 4-55346332-G-C
• MyVariant Identifiers: chr4:g.56212499G>C (hg19) ; chr4:g.55346332G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55346332G>C , CM000666.2:g.55346332G>C	GRCh38
NC_000004.11:g.56212499G>C , CM000666.1:g.56212499G>C	GRCh37
NC_000004.10:g.55907256G>C	NCBI36
NG_028230.1:g.5112G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.-5G>C MANE Select	ENSP00000264228.4:n.-5G>C
ENST00000679351.1:c.-5G>C	ENSP00000505676.1:n.-5G>C
ENST00000679707.1:c.-5G>C	ENSP00000505713.1:n.-5G>C
ENST00000679836.1:c.-5G>C	ENSP00000506601.1:n.-5G>C
ENST00000264228.8:c.-5G>C	ENSP00000264228.4:n.-5G>C
NM_024592.4:c.-5G>C	NP_078868.1:n.-5G>C
XM_005265766.2:c.-5G>C	XP_005265823.1:n.-5G>C
XM_005265767.2:c.-5G>C	XP_005265824.1:n.-5G>C
XM_005265766.4:c.-5G>C	XP_005265823.1:n.-5G>C
XM_005265767.3:c.-5G>C	XP_005265824.1:n.-5G>C
NM_024592.5:c.-5G>C MANE Select	NP_078868.1:n.-5G>C