Canonical Allele Identifier: CA374882589

Gene: NR5A1

Linked Data

• MyVariant Identifiers: chr9:g.127255402C>G (hg19) ; chr9:g.124493123C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124493123C>G , CM000671.2:g.124493123C>G	GRCh38
NC_000009.11:g.127255402C>G , CM000671.1:g.127255402C>G	GRCh37
NC_000009.10:g.126295223C>G	NCBI36
NG_008176.1:g.19298G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373588.9:c.897G>C MANE Select	ENSP00000362690.4:p.Gln299His
ENST00000373587.3:c.249G>C	ENSP00000362689.3:p.Gln83His
ENST00000373588.8:c.897G>C	ENSP00000362690.4:p.Gln299His
ENST00000620110.4:c.871-1895G>C	ENSP00000483309.1:n.871-1895G>C
NM_004959.4:c.897G>C	NP_004950.2:p.Gln299His
XM_005251871.2:c.897G>C	XP_005251928.1:p.Gln299His
XM_005251872.3:c.636G>C	XP_005251929.1:p.Gln212His
XM_011518455.1:c.897G>C	XP_011516757.1:p.Gln299His
XM_011518456.1:c.870+6967G>C	XP_011516758.1:n.870+6967G>C
NM_004959.5:c.897G>C MANE Select	NP_004950.2:p.Gln299His