Canonical Allele Identifier: CA1465408889
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740348A= , CM000666.2:g.67740348A= GRCh38
NC_000004.11:g.68606066A= , CM000666.1:g.68606066A= GRCh37
NC_000004.10:g.68288661A= NCBI36
NG_009293.1:g.20739T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*132T= MANE Select ENSP00000226413.5:n.*132T=
ENST00000226413.4:c.*132T= ENSP00000226413.4:n.*132T=
NM_000406.2:c.*132T= NP_000397.1:n.*132T=
NM_001012763.1:c.*241T= NP_001012781.1:n.*241T=
NM_000406.3:c.*132T= MANE Select NP_000397.1:n.*132T=
NM_001012763.2:c.*241T= NP_001012781.1:n.*241T=