Canonical Allele Identifier: CA2508794479
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740216T>C , CM000666.2:g.67740216T>C GRCh38
NC_000004.11:g.68605934T>C , CM000666.1:g.68605934T>C GRCh37
NC_000004.10:g.68288529T>C NCBI36
NG_009293.1:g.20871A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*264A>G MANE Select ENSP00000226413.5:n.*264A>G
ENST00000226413.4:c.*264A>G ENSP00000226413.4:n.*264A>G
NM_000406.2:c.*264A>G NP_000397.1:n.*264A>G
NM_001012763.1:c.*373A>G NP_001012781.1:n.*373A>G
NM_000406.3:c.*264A>G MANE Select NP_000397.1:n.*264A>G
NM_001012763.2:c.*373A>G NP_001012781.1:n.*373A>G