Canonical Allele Identifier: CA1465408792
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740246G= , CM000666.2:g.67740246G= GRCh38
NC_000004.11:g.68605964G= , CM000666.1:g.68605964G= GRCh37
NC_000004.10:g.68288559G= NCBI36
NG_009293.1:g.20841C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*234C= MANE Select ENSP00000226413.5:n.*234C=
ENST00000226413.4:c.*234C= ENSP00000226413.4:n.*234C=
NM_000406.2:c.*234C= NP_000397.1:n.*234C=
NM_001012763.1:c.*343C= NP_001012781.1:n.*343C=
NM_000406.3:c.*234C= MANE Select NP_000397.1:n.*234C=
NM_001012763.2:c.*343C= NP_001012781.1:n.*343C=