Canonical Allele Identifier: CA1465408899
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740355T= , CM000666.2:g.67740355T= GRCh38
NC_000004.11:g.68606073T= , CM000666.1:g.68606073T= GRCh37
NC_000004.10:g.68288668T= NCBI36
NG_009293.1:g.20732A=

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*125A= MANE Select ENSP00000226413.5:n.*125A=
ENST00000226413.4:c.*125A= ENSP00000226413.4:n.*125A=
NM_000406.2:c.*125A= NP_000397.1:n.*125A=
NM_001012763.1:c.*234A= NP_001012781.1:n.*234A=
NM_000406.3:c.*125A= MANE Select NP_000397.1:n.*125A=
NM_001012763.2:c.*234A= NP_001012781.1:n.*234A=