Canonical Allele Identifier: CA1465409309
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740735G= , CM000666.2:g.67740735G= GRCh38
NC_000004.11:g.68606453G= , CM000666.1:g.68606453G= GRCh37
NC_000004.10:g.68289048G= NCBI36
NG_009293.1:g.20352C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.743-11C= MANE Select ENSP00000226413.5:n.743-11C=
ENST00000226413.4:c.743-11C= ENSP00000226413.4:n.743-11C=
ENST00000420975.2:c.615-11C= ENSP00000397561.2:n.615-11C=
NM_000406.2:c.743-11C= NP_000397.1:n.743-11C=
NM_001012763.1:c.615-11C= NP_001012781.1:n.615-11C=
NM_000406.3:c.743-11C= MANE Select NP_000397.1:n.743-11C=
NM_001012763.2:c.615-11C= NP_001012781.1:n.615-11C=
Search 100 bp 5'
Search 100 bp 3'