Canonical Allele Identifier: CA374890878
Gene: NR5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.127265672C>A (hg19) chr9:g.124503393C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.124503393C>A , CM000671.2:g.124503393C>A GRCh38
NC_000009.11:g.127265672C>A , CM000671.1:g.127265672C>A GRCh37
NC_000009.10:g.126305493C>A NCBI36
NG_008176.1:g.9028G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373588.9:c.3G>T MANE Select ENSP00000362690.4:p.Met1Ile
ENST00000373588.8:c.3G>T ENSP00000362690.4:p.Met1Ile
ENST00000455734.1:c.3G>T ENSP00000393245.1:p.Met1Ile
ENST00000620110.4:c.3G>T ENSP00000483309.1:p.Met1Ile
NM_004959.4:c.3G>T NP_004950.2:p.Met1Ile
XM_005251871.2:c.3G>T XP_005251928.1:p.Met1Ile
XM_005251872.3:c.-117G>T XP_005251929.1:n.-117G>T
XM_011518455.1:c.3G>T XP_011516757.1:p.Met1Ile
XM_011518456.1:c.3G>T XP_011516758.1:p.Met1Ile
NM_004959.5:c.3G>T MANE Select NP_004950.2:p.Met1Ile
Search 100 bp 5'
Search 100 bp 3'