Canonical Allele Identifier: CA1465409080
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740588A= , CM000666.2:g.67740588A= GRCh38
NC_000004.11:g.68606306A= , CM000666.1:g.68606306A= GRCh37
NC_000004.10:g.68288901A= NCBI36
NG_009293.1:g.20499T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.879T= MANE Select ENSP00000226413.5:p.Asp293=
ENST00000226413.4:c.879T= ENSP00000226413.4:p.Asp293=
ENST00000420975.2:c.751T= ENSP00000397561.2:n.751T=
NM_000406.2:c.879T= NP_000397.1:p.Asp293=
NM_001012763.1:c.*1T= NP_001012781.1:n.*1T=
NM_000406.3:c.879T= MANE Select NP_000397.1:p.Asp293=
NM_001012763.2:c.*1T= NP_001012781.1:n.*1T=
Search 100 bp 5'
Search 100 bp 3'