Canonical Allele Identifier: CA1465408732
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740182A= , CM000666.2:g.67740182A= GRCh38
NC_000004.11:g.68605900A= , CM000666.1:g.68605900A= GRCh37
NC_000004.10:g.68288495A= NCBI36
NG_009293.1:g.20905T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*298T= MANE Select ENSP00000226413.5:n.*298T=
ENST00000226413.4:c.*298T= ENSP00000226413.4:n.*298T=
NM_000406.2:c.*298T= NP_000397.1:n.*298T=
NM_001012763.1:c.*407T= NP_001012781.1:n.*407T=
NM_000406.3:c.*298T= MANE Select NP_000397.1:n.*298T=
NM_001012763.2:c.*407T= NP_001012781.1:n.*407T=