Canonical Allele Identifier: CA374890229

Gene: NR5A1

Linked Data

• gnomAD v4: 9-124503118-G-T
• MyVariant Identifiers: chr9:g.127265397G>T (hg19) ; chr9:g.124503118G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124503118G>T , CM000671.2:g.124503118G>T	GRCh38
NC_000009.11:g.127265397G>T , CM000671.1:g.127265397G>T	GRCh37
NC_000009.10:g.126305218G>T	NCBI36
NG_008176.1:g.9303C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373588.9:c.205C>A MANE Select	ENSP00000362690.4:p.Arg69Ser
ENST00000373588.8:c.205C>A	ENSP00000362690.4:p.Arg69Ser
ENST00000455734.1:c.205C>A	ENSP00000393245.1:p.Arg69Ser
ENST00000620110.4:c.205C>A	ENSP00000483309.1:p.Arg69Ser
NM_004959.4:c.205C>A	NP_004950.2:p.Arg69Ser
XM_005251871.2:c.205C>A	XP_005251928.1:p.Arg69Ser
XM_005251872.3:c.-18+176C>A	XP_005251929.1:n.-18+176C>A
XM_011518455.1:c.205C>A	XP_011516757.1:p.Arg69Ser
XM_011518456.1:c.205C>A	XP_011516758.1:p.Arg69Ser
NM_004959.5:c.205C>A MANE Select	NP_004950.2:p.Arg69Ser