Canonical Allele Identifier: CA797693280
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1239856094

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740322G>A , CM000666.2:g.67740322G>A GRCh38
NC_000004.11:g.68606040G>A , CM000666.1:g.68606040G>A GRCh37
NC_000004.10:g.68288635G>A NCBI36
NG_009293.1:g.20765C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*158C>T MANE Select ENSP00000226413.5:n.*158C>T
ENST00000226413.4:c.*158C>T ENSP00000226413.4:n.*158C>T
NM_000406.2:c.*158C>T NP_000397.1:n.*158C>T
NM_001012763.1:c.*267C>T NP_001012781.1:n.*267C>T
NM_000406.3:c.*158C>T MANE Select NP_000397.1:n.*158C>T
NM_001012763.2:c.*267C>T NP_001012781.1:n.*267C>T