Canonical Allele Identifier: CA796421296

Gene: SRD5A3

Linked Data

• dbSNP Id: rs1290897552
• gnomAD v3: 4-55359639-C-G
• gnomAD v4: 4-55359639-C-G
• MyVariant Identifiers: chr4:g.56225806C>G (hg19) ; chr4:g.55359639C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359639C>G , CM000666.2:g.55359639C>G	GRCh38
NC_000004.11:g.56225806C>G , CM000666.1:g.56225806C>G	GRCh37
NC_000004.10:g.55920563C>G	NCBI36
NG_028230.1:g.18419C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.364+151C>G MANE Select	ENSP00000264228.4:n.364+151C>G
ENST00000677177.2:c.77+151C>G
ENST00000678717.1:n.261+151C>G
ENST00000679351.1:c.364+151C>G	ENSP00000505676.1:n.364+151C>G
ENST00000679707.1:c.364+151C>G	ENSP00000505713.1:n.364+151C>G
ENST00000679836.1:c.364+151C>G	ENSP00000506601.1:n.364+151C>G
ENST00000680700.1:c.364+151C>G	ENSP00000504926.1:n.364+151C>G
ENST00000264228.8:c.364+151C>G	ENSP00000264228.4:n.364+151C>G
ENST00000505210.1:c.289+151C>G	ENSP00000424714.1:n.289+151C>G
ENST00000514398.1:n.373+151C>G
NM_024592.4:c.364+151C>G	NP_078868.1:n.364+151C>G
XM_005265766.2:c.364+151C>G	XP_005265823.1:n.364+151C>G
XM_005265767.2:c.364+151C>G	XP_005265824.1:n.364+151C>G
XM_005265766.4:c.364+151C>G	XP_005265823.1:n.364+151C>G
XM_005265767.3:c.364+151C>G	XP_005265824.1:n.364+151C>G
XM_017008601.1:c.229+151C>G	XP_016864090.1:n.229+151C>G
NM_024592.5:c.364+151C>G MANE Select	NP_078868.1:n.364+151C>G