Canonical Allele Identifier: CA1465408868
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740314T= , CM000666.2:g.67740314T= GRCh38
NC_000004.11:g.68606032T= , CM000666.1:g.68606032T= GRCh37
NC_000004.10:g.68288627T= NCBI36
NG_009293.1:g.20773A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*166A= MANE Select ENSP00000226413.5:n.*166A=
ENST00000226413.4:c.*166A= ENSP00000226413.4:n.*166A=
NM_000406.2:c.*166A= NP_000397.1:n.*166A=
NM_001012763.1:c.*275A= NP_001012781.1:n.*275A=
NM_000406.3:c.*166A= MANE Select NP_000397.1:n.*166A=
NM_001012763.2:c.*275A= NP_001012781.1:n.*275A=