Canonical Allele Identifier: CA1465408755
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740202A= , CM000666.2:g.67740202A= GRCh38
NC_000004.11:g.68605920A= , CM000666.1:g.68605920A= GRCh37
NC_000004.10:g.68288515A= NCBI36
NG_009293.1:g.20885T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*278T= MANE Select ENSP00000226413.5:n.*278T=
ENST00000226413.4:c.*278T= ENSP00000226413.4:n.*278T=
NM_000406.2:c.*278T= NP_000397.1:n.*278T=
NM_001012763.1:c.*387T= NP_001012781.1:n.*387T=
NM_000406.3:c.*278T= MANE Select NP_000397.1:n.*278T=
NM_001012763.2:c.*387T= NP_001012781.1:n.*387T=