Canonical Allele Identifier: CA1465409306
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740733T= , CM000666.2:g.67740733T= GRCh38
NC_000004.11:g.68606451T= , CM000666.1:g.68606451T= GRCh37
NC_000004.10:g.68289046T= NCBI36
NG_009293.1:g.20354A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.743-9A= MANE Select ENSP00000226413.5:n.743-9A=
ENST00000226413.4:c.743-9A= ENSP00000226413.4:n.743-9A=
ENST00000420975.2:c.615-9A= ENSP00000397561.2:n.615-9A=
NM_000406.2:c.743-9A= NP_000397.1:n.743-9A=
NM_001012763.1:c.615-9A= NP_001012781.1:n.615-9A=
NM_000406.3:c.743-9A= MANE Select NP_000397.1:n.743-9A=
NM_001012763.2:c.615-9A= NP_001012781.1:n.615-9A=