Canonical Allele Identifier: CA1465409132
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740634A= , CM000666.2:g.67740634A= GRCh38
NC_000004.11:g.68606352A= , CM000666.1:g.68606352A= GRCh37
NC_000004.10:g.68288947A= NCBI36
NG_009293.1:g.20453T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.833T= MANE Select ENSP00000226413.5:p.Val278=
ENST00000226413.4:c.833T= ENSP00000226413.4:p.Val278=
ENST00000420975.2:c.705T= ENSP00000397561.2:p.Cys235=
NM_000406.2:c.833T= NP_000397.1:p.Val278=
NM_001012763.1:c.705T= NP_001012781.1:p.Cys235=
NM_000406.3:c.833T= MANE Select NP_000397.1:p.Val278=
NM_001012763.2:c.705T= NP_001012781.1:p.Cys235=
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