Canonical Allele Identifier: CA357047772
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606335A>G (hg19) chr4:g.67740617A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740617A>G , CM000666.2:g.67740617A>G GRCh38
NC_000004.11:g.68606335A>G , CM000666.1:g.68606335A>G GRCh37
NC_000004.10:g.68288930A>G NCBI36
NG_009293.1:g.20470T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.850T>C MANE Select ENSP00000226413.5:p.Tyr284His
ENST00000226413.4:c.850T>C ENSP00000226413.4:p.Tyr284His
ENST00000420975.2:c.722T>C ENSP00000397561.2:p.Leu241Pro
NM_000406.2:c.850T>C NP_000397.1:p.Tyr284His
NM_001012763.1:c.722T>C NP_001012781.1:p.Leu241Pro
NM_000406.3:c.850T>C MANE Select NP_000397.1:p.Tyr284His
NM_001012763.2:c.722T>C NP_001012781.1:p.Leu241Pro
Search 100 bp 5'
Search 100 bp 3'