Canonical Allele Identifier: CA1465408870
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740321T= , CM000666.2:g.67740321T= GRCh38
NC_000004.11:g.68606039T= , CM000666.1:g.68606039T= GRCh37
NC_000004.10:g.68288634T= NCBI36
NG_009293.1:g.20766A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*159A= MANE Select ENSP00000226413.5:n.*159A=
ENST00000226413.4:c.*159A= ENSP00000226413.4:n.*159A=
NM_000406.2:c.*159A= NP_000397.1:n.*159A=
NM_001012763.1:c.*268A= NP_001012781.1:n.*268A=
NM_000406.3:c.*159A= MANE Select NP_000397.1:n.*159A=
NM_001012763.2:c.*268A= NP_001012781.1:n.*268A=