Canonical Allele Identifier: CA1465408748
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740200A= , CM000666.2:g.67740200A= GRCh38
NC_000004.11:g.68605918A= , CM000666.1:g.68605918A= GRCh37
NC_000004.10:g.68288513A= NCBI36
NG_009293.1:g.20887T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*280T= MANE Select ENSP00000226413.5:n.*280T=
ENST00000226413.4:c.*280T= ENSP00000226413.4:n.*280T=
NM_000406.2:c.*280T= NP_000397.1:n.*280T=
NM_001012763.1:c.*389T= NP_001012781.1:n.*389T=
NM_000406.3:c.*280T= MANE Select NP_000397.1:n.*280T=
NM_001012763.2:c.*389T= NP_001012781.1:n.*389T=