Canonical Allele Identifier: CA1465420872
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754071A= , CM000666.2:g.67754071A= GRCh38
NC_000004.11:g.68619789A= , CM000666.1:g.68619789A= GRCh37
NC_000004.10:g.68302384A= NCBI36
NG_009293.1:g.7016T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.265T= MANE Select ENSP00000226413.5:p.Leu89=
ENST00000226413.4:c.265T= ENSP00000226413.4:p.Leu89=
ENST00000420975.2:c.265T= ENSP00000397561.2:p.Leu89=
NM_000406.2:c.265T= NP_000397.1:p.Leu89=
NM_001012763.1:c.265T= NP_001012781.1:p.Leu89=
NM_000406.3:c.265T= MANE Select NP_000397.1:p.Leu89=
NM_001012763.2:c.265T= NP_001012781.1:p.Leu89=