Canonical Allele Identifier: CA796416506

Gene: SRD5A3

Linked Data

• dbSNP Id: rs1473183586
• gnomAD v3: 4-55346266-C-G
• gnomAD v4: 4-55346266-C-G
• MyVariant Identifiers: chr4:g.56212433C>G (hg19) ; chr4:g.55346266C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55346266C>G , CM000666.2:g.55346266C>G	GRCh38
NC_000004.11:g.56212433C>G , CM000666.1:g.56212433C>G	GRCh37
NC_000004.10:g.55907190C>G	NCBI36
NG_028230.1:g.5046C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.-71C>G MANE Select	ENSP00000264228.4:n.-71C>G
ENST00000679707.1:c.-71C>G	ENSP00000505713.1:n.-71C>G
ENST00000679836.1:c.-71C>G	ENSP00000506601.1:n.-71C>G
ENST00000264228.8:c.-71C>G	ENSP00000264228.4:n.-71C>G
NM_024592.4:c.-71C>G	NP_078868.1:n.-71C>G
XM_005265766.2:c.-71C>G	XP_005265823.1:n.-71C>G
XM_005265767.2:c.-71C>G	XP_005265824.1:n.-71C>G
XM_005265766.4:c.-71C>G	XP_005265823.1:n.-71C>G
XM_005265767.3:c.-71C>G	XP_005265824.1:n.-71C>G
NM_024592.5:c.-71C>G MANE Select	NP_078868.1:n.-71C>G