Canonical Allele Identifier: CA1465420740
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754005C= , CM000666.2:g.67754005C= GRCh38
NC_000004.11:g.68619723C= , CM000666.1:g.68619723C= GRCh37
NC_000004.10:g.68302318C= NCBI36
NG_009293.1:g.7082G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.331G= MANE Select ENSP00000226413.5:p.Glu111=
ENST00000226413.4:c.331G= ENSP00000226413.4:p.Glu111=
ENST00000420975.2:c.331G= ENSP00000397561.2:p.Glu111=
NM_000406.2:c.331G= NP_000397.1:p.Glu111=
NM_001012763.1:c.331G= NP_001012781.1:p.Glu111=
NM_000406.3:c.331G= MANE Select NP_000397.1:p.Glu111=
NM_001012763.2:c.331G= NP_001012781.1:p.Glu111=