Canonical Allele Identifier: CA199731373

Gene: NR5A1

Linked Data

• dbSNP Id: rs989611741
• MyVariant Identifiers: chr9:g.124503402G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124503402G>C , CM000671.2:g.124503402G>C	GRCh38
NC_000009.11:g.127265681G>C , CM000671.1:g.127265681G>C	GRCh37
NC_000009.10:g.126305502G>C	NCBI36
NG_008176.1:g.9019C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.-7C>G MANE Select	ENSP00000362690.4:n.-7C>G
ENST00000373588.8:c.-7C>G	ENSP00000362690.4:n.-7C>G
ENST00000455734.1:c.-7C>G	ENSP00000393245.1:n.-7C>G
ENST00000620110.4:c.-7C>G	ENSP00000483309.1:n.-7C>G
NM_004959.4:c.-7C>G	NP_004950.2:n.-7C>G
XM_005251871.2:c.-7C>G	XP_005251928.1:n.-7C>G
XM_005251872.3:c.-126C>G	XP_005251929.1:n.-126C>G
XM_011518455.1:c.-7C>G	XP_011516757.1:n.-7C>G
XM_011518456.1:c.-7C>G	XP_011516758.1:n.-7C>G
NM_004959.5:c.-7C>G MANE Select	NP_004950.2:n.-7C>G