Canonical Allele Identifier: CA796416497

Gene: SRD5A3

Linked Data

• dbSNP Id: rs1388567835
• gnomAD v4: 4-55346263-G-A
• MyVariant Identifiers: chr4:g.56212430G>A (hg19) ; chr4:g.55346263G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55346263G>A , CM000666.2:g.55346263G>A	GRCh38
NC_000004.11:g.56212430G>A , CM000666.1:g.56212430G>A	GRCh37
NC_000004.10:g.55907187G>A	NCBI36
NG_028230.1:g.5043G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.-74G>A MANE Select	ENSP00000264228.4:n.-74G>A
ENST00000679707.1:c.-74G>A	ENSP00000505713.1:n.-74G>A
ENST00000679836.1:c.-74G>A	ENSP00000506601.1:n.-74G>A
ENST00000264228.8:c.-74G>A	ENSP00000264228.4:n.-74G>A
NM_024592.4:c.-74G>A	NP_078868.1:n.-74G>A
XM_005265766.2:c.-74G>A	XP_005265823.1:n.-74G>A
XM_005265767.2:c.-74G>A	XP_005265824.1:n.-74G>A
XM_005265766.4:c.-74G>A	XP_005265823.1:n.-74G>A
XM_005265767.3:c.-74G>A	XP_005265824.1:n.-74G>A
NM_024592.5:c.-74G>A MANE Select	NP_078868.1:n.-74G>A