Canonical Allele Identifier: CA35913339

Gene: NR5A2

Linked Data

• dbSNP Id: rs1002860480
• gnomAD v3: 1-200038192-T-A
• gnomAD v4: 1-200038192-T-A
• MyVariant Identifiers: chr1:g.200007320T>A (hg19) ; chr1:g.200038192T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200038192T>A , CM000663.2:g.200038192T>A	GRCh38
NC_000001.10:g.200007320T>A , CM000663.1:g.200007320T>A	GRCh37
NC_000001.9:g.198273943T>A	NCBI36
NG_050913.1:g.15591T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367362.8:c.65-1466T>A MANE Select	ENSP00000356331.3:n.65-1466T>A
ENST00000236914.7:c.65-5582T>A	ENSP00000236914.3:n.65-5582T>A
ENST00000367362.7:c.65-1466T>A	ENSP00000356331.3:n.65-1466T>A
ENST00000447034.1:c.30-509T>A
ENST00000474307.1:c.*419-5582T>A	ENSP00000436776.1:n.*419-5582T>A
NM_003822.4:c.65-5582T>A	NP_003813.1:n.65-5582T>A
NM_205860.2:c.65-1466T>A	NP_995582.1:n.65-1466T>A
XM_011509380.1:c.-56-1466T>A	XP_011507682.1:n.-56-1466T>A
XM_011509382.1:c.-14-5582T>A	XP_011507684.1:n.-14-5582T>A
XM_011509381.3:c.-637T>A	XP_011507683.1:n.-637T>A
NM_205860.3:c.65-1466T>A MANE Select	NP_995582.1:n.65-1466T>A
NM_003822.5:c.65-5582T>A	NP_003813.1:n.65-5582T>A