Canonical Allele Identifier: CA1465408872
Gene: GNRHR HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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