Canonical Allele Identifier: CA1465408630
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740089A= , CM000666.2:g.67740089A= GRCh38
NC_000004.11:g.68605807A= , CM000666.1:g.68605807A= GRCh37
NC_000004.10:g.68288402A= NCBI36
NG_009293.1:g.20998T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*391T= MANE Select ENSP00000226413.5:n.*391T=
ENST00000226413.4:c.*391T= ENSP00000226413.4:n.*391T=
NM_000406.2:c.*391T= NP_000397.1:n.*391T=
NM_001012763.1:c.*500T= NP_001012781.1:n.*500T=
NM_000406.3:c.*391T= MANE Select NP_000397.1:n.*391T=
NM_001012763.2:c.*500T= NP_001012781.1:n.*500T=
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