Canonical Allele Identifier: CA1465408849
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740299C= , CM000666.2:g.67740299C= GRCh38
NC_000004.11:g.68606017C= , CM000666.1:g.68606017C= GRCh37
NC_000004.10:g.68288612C= NCBI36
NG_009293.1:g.20788G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*181G= MANE Select ENSP00000226413.5:n.*181G=
ENST00000226413.4:c.*181G= ENSP00000226413.4:n.*181G=
NM_000406.2:c.*181G= NP_000397.1:n.*181G=
NM_001012763.1:c.*290G= NP_001012781.1:n.*290G=
NM_000406.3:c.*181G= MANE Select NP_000397.1:n.*181G=
NM_001012763.2:c.*290G= NP_001012781.1:n.*290G=