Canonical Allele Identifier: CA1465420857
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754064G= , CM000666.2:g.67754064G= GRCh38
NC_000004.11:g.68619782G= , CM000666.1:g.68619782G= GRCh37
NC_000004.10:g.68302377G= NCBI36
NG_009293.1:g.7023C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.272C= MANE Select ENSP00000226413.5:p.Thr91=
ENST00000226413.4:c.272C= ENSP00000226413.4:p.Thr91=
ENST00000420975.2:c.272C= ENSP00000397561.2:p.Thr91=
NM_000406.2:c.272C= NP_000397.1:p.Thr91=
NM_001012763.1:c.272C= NP_001012781.1:p.Thr91=
NM_000406.3:c.272C= MANE Select NP_000397.1:p.Thr91=
NM_001012763.2:c.272C= NP_001012781.1:p.Thr91=
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