Canonical Allele Identifier: CA1465420807
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754048T= , CM000666.2:g.67754048T= GRCh38
NC_000004.11:g.68619766T= , CM000666.1:g.68619766T= GRCh37
NC_000004.10:g.68302361T= NCBI36
NG_009293.1:g.7039A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.288A= MANE Select ENSP00000226413.5:p.Pro96=
ENST00000226413.4:c.288A= ENSP00000226413.4:p.Pro96=
ENST00000420975.2:c.288A= ENSP00000397561.2:p.Pro96=
NM_000406.2:c.288A= NP_000397.1:p.Pro96=
NM_001012763.1:c.288A= NP_001012781.1:p.Pro96=
NM_000406.3:c.288A= MANE Select NP_000397.1:p.Pro96=
NM_001012763.2:c.288A= NP_001012781.1:p.Pro96=