Canonical Allele Identifier: CA35913653

Gene: NR5A2

Linked Data

• dbSNP Id: rs910592652
• MyVariant Identifiers: chr1:g.200007685A>G (hg19) ; chr1:g.200038557A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200038557A>G , CM000663.2:g.200038557A>G	GRCh38
NC_000001.10:g.200007685A>G , CM000663.1:g.200007685A>G	GRCh37
NC_000001.9:g.198274308A>G	NCBI36
NG_050913.1:g.15956A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367362.8:c.65-1101A>G MANE Select	ENSP00000356331.3:n.65-1101A>G
ENST00000236914.7:c.65-5217A>G	ENSP00000236914.3:n.65-5217A>G
ENST00000367362.7:c.65-1101A>G	ENSP00000356331.3:n.65-1101A>G
ENST00000447034.1:c.30-144A>G
ENST00000474307.1:c.*419-5217A>G	ENSP00000436776.1:n.*419-5217A>G
NM_003822.4:c.65-5217A>G	NP_003813.1:n.65-5217A>G
NM_205860.2:c.65-1101A>G	NP_995582.1:n.65-1101A>G
XM_011509380.1:c.-56-1101A>G	XP_011507682.1:n.-56-1101A>G
XM_011509382.1:c.-14-5217A>G	XP_011507684.1:n.-14-5217A>G
XM_011509381.3:c.-272A>G	XP_011507683.1:n.-272A>G
NM_205860.3:c.65-1101A>G MANE Select	NP_995582.1:n.65-1101A>G
NM_003822.5:c.65-5217A>G	NP_003813.1:n.65-5217A>G