Canonical Allele Identifier: CA1465421041
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754377A= , CM000666.2:g.67754377A= GRCh38
NC_000004.11:g.68620095A= , CM000666.1:g.68620095A= GRCh37
NC_000004.10:g.68302690A= NCBI36
NG_009293.1:g.6710T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-42T= MANE Select ENSP00000226413.5:n.-42T=
NM_000406.2:c.-42T= NP_000397.1:n.-42T=
NM_001012763.1:c.-42T= NP_001012781.1:n.-42T=
NM_000406.3:c.-42T= MANE Select NP_000397.1:n.-42T=
NM_001012763.2:c.-42T= NP_001012781.1:n.-42T=