Canonical Allele Identifier: CA1465408774
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1022837529
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740221A>C , CM000666.2:g.67740221A>C GRCh38
NC_000004.11:g.68605939A>C , CM000666.1:g.68605939A>C GRCh37
NC_000004.10:g.68288534A>C NCBI36
NG_009293.1:g.20866T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*259T>G MANE Select ENSP00000226413.5:n.*259T>G
ENST00000226413.4:c.*259T>G ENSP00000226413.4:n.*259T>G
NM_000406.2:c.*259T>G NP_000397.1:n.*259T>G
NM_001012763.1:c.*368T>G NP_001012781.1:n.*368T>G
NM_000406.3:c.*259T>G MANE Select NP_000397.1:n.*259T>G
NM_001012763.2:c.*368T>G NP_001012781.1:n.*368T>G
Search 100 bp 5'
Search 100 bp 3'