Canonical Allele Identifier: CA1465408708
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740141G= , CM000666.2:g.67740141G= GRCh38
NC_000004.11:g.68605859G= , CM000666.1:g.68605859G= GRCh37
NC_000004.10:g.68288454G= NCBI36
NG_009293.1:g.20946C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*339C= MANE Select ENSP00000226413.5:n.*339C=
ENST00000226413.4:c.*339C= ENSP00000226413.4:n.*339C=
NM_000406.2:c.*339C= NP_000397.1:n.*339C=
NM_001012763.1:c.*448C= NP_001012781.1:n.*448C=
NM_000406.3:c.*339C= MANE Select NP_000397.1:n.*339C=
NM_001012763.2:c.*448C= NP_001012781.1:n.*448C=
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