Canonical Allele Identifier: CA374890227

Gene: NR5A1

Linked Data

• ClinVar Variation Id: 2136807
• ClinVar RCV Id: RCV003062229
• MyVariant Identifiers: chr9:g.127265397G>C (hg19) ; chr9:g.124503118G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124503118G>C , CM000671.2:g.124503118G>C	GRCh38
NC_000009.11:g.127265397G>C , CM000671.1:g.127265397G>C	GRCh37
NC_000009.10:g.126305218G>C	NCBI36
NG_008176.1:g.9303C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373588.9:c.205C>G MANE Select	ENSP00000362690.4:p.Arg69Gly
ENST00000373588.8:c.205C>G	ENSP00000362690.4:p.Arg69Gly
ENST00000455734.1:c.205C>G	ENSP00000393245.1:p.Arg69Gly
ENST00000620110.4:c.205C>G	ENSP00000483309.1:p.Arg69Gly
NM_004959.4:c.205C>G	NP_004950.2:p.Arg69Gly
XM_005251871.2:c.205C>G	XP_005251928.1:p.Arg69Gly
XM_005251872.3:c.-18+176C>G	XP_005251929.1:n.-18+176C>G
XM_011518455.1:c.205C>G	XP_011516757.1:p.Arg69Gly
XM_011518456.1:c.205C>G	XP_011516758.1:p.Arg69Gly
NM_004959.5:c.205C>G MANE Select	NP_004950.2:p.Arg69Gly