Canonical Allele Identifier: CA467208475

Gene: NR5A1

Linked Data

• dbSNP Id: rs1300488730
• gnomAD v2: 9-127265482-C-T
• gnomAD v4: 9-124503203-C-T
• COSMIC: COSM4795138
• MyVariant Identifiers: chr9:g.127265482C>T (hg19) ; chr9:g.124503203C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124503203C>T , CM000671.2:g.124503203C>T	GRCh38
NC_000009.11:g.127265482C>T , CM000671.1:g.127265482C>T	GRCh37
NC_000009.10:g.126305303C>T	NCBI36
NG_008176.1:g.9218G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.120G>A MANE Select	ENSP00000362690.4:p.Thr40=
ENST00000373588.8:c.120G>A	ENSP00000362690.4:p.Thr40=
ENST00000455734.1:c.120G>A	ENSP00000393245.1:p.Thr40=
ENST00000620110.4:c.120G>A	ENSP00000483309.1:p.Thr40=
NM_004959.4:c.120G>A	NP_004950.2:p.Thr40=
XM_005251871.2:c.120G>A	XP_005251928.1:p.Thr40=
XM_005251872.3:c.-18+91G>A	XP_005251929.1:n.-18+91G>A
XM_011518455.1:c.120G>A	XP_011516757.1:p.Thr40=
XM_011518456.1:c.120G>A	XP_011516758.1:p.Thr40=
NM_004959.5:c.120G>A MANE Select	NP_004950.2:p.Thr40=