Canonical Allele Identifier: CA5235411

Gene: NR5A1

Linked Data

• dbSNP Id: rs755684996
• ExAC: 9:127262516 C / T
• gnomAD v2: 9-127262516-C-T
• gnomAD v4: 9-124500237-C-T
• MyVariant Identifiers: chr9:g.127262516C>T (hg19) ; chr9:g.124500237C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124500237C>T , CM000671.2:g.124500237C>T	GRCh38
NC_000009.11:g.127262516C>T , CM000671.1:g.127262516C>T	GRCh37
NC_000009.10:g.126302337C>T	NCBI36
NG_008176.1:g.12184G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373588.9:c.723G>A MANE Select	ENSP00000362690.4:p.Arg241=
ENST00000373587.3:c.75G>A	ENSP00000362689.3:p.Arg25=
ENST00000373588.8:c.723G>A	ENSP00000362690.4:p.Arg241=
ENST00000620110.4:c.723G>A	ENSP00000483309.1:p.Arg241=
NM_004959.4:c.723G>A	NP_004950.2:p.Arg241=
XM_005251871.2:c.723G>A	XP_005251928.1:p.Arg241=
XM_005251872.3:c.462G>A	XP_005251929.1:p.Arg154=
XM_011518455.1:c.723G>A	XP_011516757.1:p.Arg241=
XM_011518456.1:c.723G>A	XP_011516758.1:p.Arg241=
NM_004959.5:c.723G>A MANE Select	NP_004950.2:p.Arg241=