Canonical Allele Identifier: CA1465408901
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740358C= , CM000666.2:g.67740358C= GRCh38
NC_000004.11:g.68606076C= , CM000666.1:g.68606076C= GRCh37
NC_000004.10:g.68288671C= NCBI36
NG_009293.1:g.20729G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*122G= MANE Select ENSP00000226413.5:n.*122G=
ENST00000226413.4:c.*122G= ENSP00000226413.4:n.*122G=
NM_000406.2:c.*122G= NP_000397.1:n.*122G=
NM_001012763.1:c.*231G= NP_001012781.1:n.*231G=
NM_000406.3:c.*122G= MANE Select NP_000397.1:n.*122G=
NM_001012763.2:c.*231G= NP_001012781.1:n.*231G=