Canonical Allele Identifier: CA1465408907
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740362A= , CM000666.2:g.67740362A= GRCh38
NC_000004.11:g.68606080A= , CM000666.1:g.68606080A= GRCh37
NC_000004.10:g.68288675A= NCBI36
NG_009293.1:g.20725T=

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*118T= MANE Select ENSP00000226413.5:n.*118T=
ENST00000226413.4:c.*118T= ENSP00000226413.4:n.*118T=
NM_000406.2:c.*118T= NP_000397.1:n.*118T=
NM_001012763.1:c.*227T= NP_001012781.1:n.*227T=
NM_000406.3:c.*118T= MANE Select NP_000397.1:n.*118T=
NM_001012763.2:c.*227T= NP_001012781.1:n.*227T=