Canonical Allele Identifier: CA590936723

Gene: NR5A1

Linked Data

• dbSNP Id: rs1463182647
• gnomAD v2: 9-127265512-A-G
• gnomAD v4: 9-124503233-A-G
• MyVariant Identifiers: chr9:g.127265512A>G (hg19) ; chr9:g.124503233A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124503233A>G , CM000671.2:g.124503233A>G	GRCh38
NC_000009.11:g.127265512A>G , CM000671.1:g.127265512A>G	GRCh37
NC_000009.10:g.126305333A>G	NCBI36
NG_008176.1:g.9188T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.103-13T>C MANE Select	ENSP00000362690.4:n.103-13T>C
ENST00000373588.8:c.103-13T>C	ENSP00000362690.4:n.103-13T>C
ENST00000455734.1:c.103-13T>C	ENSP00000393245.1:n.103-13T>C
ENST00000620110.4:c.103-13T>C	ENSP00000483309.1:n.103-13T>C
NM_004959.4:c.103-13T>C	NP_004950.2:n.103-13T>C
XM_005251871.2:c.103-13T>C	XP_005251928.1:n.103-13T>C
XM_005251872.3:c.-18+61T>C	XP_005251929.1:n.-18+61T>C
XM_011518455.1:c.103-13T>C	XP_011516757.1:n.103-13T>C
XM_011518456.1:c.103-13T>C	XP_011516758.1:n.103-13T>C
NM_004959.5:c.103-13T>C MANE Select	NP_004950.2:n.103-13T>C