Canonical Allele Identifier: CA199722387

Gene: NR5A1

Linked Data

• dbSNP Id: rs892800744
• gnomAD v3: 9-124492978-T-C
• gnomAD v4: 9-124492978-T-C
• MyVariant Identifiers: chr9:g.127255257T>C (hg19) ; chr9:g.124492978T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124492978T>C , CM000671.2:g.124492978T>C	GRCh38
NC_000009.11:g.127255257T>C , CM000671.1:g.127255257T>C	GRCh37
NC_000009.10:g.126295078T>C	NCBI36
NG_008176.1:g.19443A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.990+52A>G MANE Select	ENSP00000362690.4:n.990+52A>G
ENST00000373587.3:c.342+52A>G	ENSP00000362689.3:n.342+52A>G
ENST00000373588.8:c.990+52A>G	ENSP00000362690.4:n.990+52A>G
ENST00000620110.4:c.871-1750A>G	ENSP00000483309.1:n.871-1750A>G
NM_004959.4:c.990+52A>G	NP_004950.2:n.990+52A>G
XM_005251871.2:c.990+52A>G	XP_005251928.1:n.990+52A>G
XM_005251872.3:c.729+52A>G	XP_005251929.1:n.729+52A>G
XM_011518455.1:c.990+52A>G	XP_011516757.1:n.990+52A>G
XM_011518456.1:c.870+7112A>G	XP_011516758.1:n.870+7112A>G
NM_004959.5:c.990+52A>G MANE Select	NP_004950.2:n.990+52A>G