Canonical Allele Identifier: CA1465408775
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740222A= , CM000666.2:g.67740222A= GRCh38
NC_000004.11:g.68605940A= , CM000666.1:g.68605940A= GRCh37
NC_000004.10:g.68288535A= NCBI36
NG_009293.1:g.20865T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*258T= MANE Select ENSP00000226413.5:n.*258T=
ENST00000226413.4:c.*258T= ENSP00000226413.4:n.*258T=
NM_000406.2:c.*258T= NP_000397.1:n.*258T=
NM_001012763.1:c.*367T= NP_001012781.1:n.*367T=
NM_000406.3:c.*258T= MANE Select NP_000397.1:n.*258T=
NM_001012763.2:c.*367T= NP_001012781.1:n.*367T=