Canonical Allele Identifier: CA374890740

Gene: NR5A1

Linked Data

• dbSNP Id: rs1207885611
• gnomAD v2: 9-127265619-T-C
• gnomAD v4: 9-124503340-T-C
• MyVariant Identifiers: chr9:g.127265619T>C (hg19) ; chr9:g.124503340T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124503340T>C , CM000671.2:g.124503340T>C	GRCh38
NC_000009.11:g.127265619T>C , CM000671.1:g.127265619T>C	GRCh37
NC_000009.10:g.126305440T>C	NCBI36
NG_008176.1:g.9081A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.56A>G MANE Select	ENSP00000362690.4:p.Lys19Arg
ENST00000373588.8:c.56A>G	ENSP00000362690.4:p.Lys19Arg
ENST00000455734.1:c.56A>G	ENSP00000393245.1:p.Lys19Arg
ENST00000620110.4:c.56A>G	ENSP00000483309.1:p.Lys19Arg
NM_004959.4:c.56A>G	NP_004950.2:p.Lys19Arg
XM_005251871.2:c.56A>G	XP_005251928.1:p.Lys19Arg
XM_005251872.3:c.-64A>G	XP_005251929.1:n.-64A>G
XM_011518455.1:c.56A>G	XP_011516757.1:p.Lys19Arg
XM_011518456.1:c.56A>G	XP_011516758.1:p.Lys19Arg
NM_004959.5:c.56A>G MANE Select	NP_004950.2:p.Lys19Arg