Canonical Allele Identifier: CA1465421050
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754387T= , CM000666.2:g.67754387T= GRCh38
NC_000004.11:g.68620105T= , CM000666.1:g.68620105T= GRCh37
NC_000004.10:g.68302700T= NCBI36
NG_009293.1:g.6700A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-52A= MANE Select ENSP00000226413.5:n.-52A=
NM_000406.2:c.-52A= NP_000397.1:n.-52A=
NM_001012763.1:c.-52A= NP_001012781.1:n.-52A=
NM_000406.3:c.-52A= MANE Select NP_000397.1:n.-52A=
NM_001012763.2:c.-52A= NP_001012781.1:n.-52A=