Canonical Allele Identifier: CA467208388

Gene: NR5A1

Linked Data

• dbSNP Id: rs1338841456
• gnomAD v2: 9-127262660-G-A
• gnomAD v4: 9-124500381-G-A
• MyVariant Identifiers: chr9:g.127262660G>A (hg19) ; chr9:g.124500381G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124500381G>A , CM000671.2:g.124500381G>A	GRCh38
NC_000009.11:g.127262660G>A , CM000671.1:g.127262660G>A	GRCh37
NC_000009.10:g.126302481G>A	NCBI36
NG_008176.1:g.12040C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.579C>T MANE Select	ENSP00000362690.4:p.Ile193=
ENST00000373587.3:c.40-109C>T	ENSP00000362689.3:n.40-109C>T
ENST00000373588.8:c.579C>T	ENSP00000362690.4:p.Ile193=
ENST00000620110.4:c.579C>T	ENSP00000483309.1:p.Ile193=
NM_004959.4:c.579C>T	NP_004950.2:p.Ile193=
XM_005251871.2:c.579C>T	XP_005251928.1:p.Ile193=
XM_005251872.3:c.318C>T	XP_005251929.1:p.Ile106=
XM_011518455.1:c.579C>T	XP_011516757.1:p.Ile193=
XM_011518456.1:c.579C>T	XP_011516758.1:p.Ile193=
NM_004959.5:c.579C>T MANE Select	NP_004950.2:p.Ile193=