Canonical Allele Identifier: CA1465420318
Gene: GNRHR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753704C= , CM000666.2:g.67753704C= GRCh38
NC_000004.11:g.68619422C= , CM000666.1:g.68619422C= GRCh37
NC_000004.10:g.68302017C= NCBI36
NG_009293.1:g.7383G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.522+110G= MANE Select ENSP00000226413.5:n.522+110G=
ENST00000226413.4:c.522+110G= ENSP00000226413.4:n.522+110G=
ENST00000420975.2:c.522+110G= ENSP00000397561.2:n.522+110G=
NM_000406.2:c.522+110G= NP_000397.1:n.522+110G=
NM_001012763.1:c.522+110G= NP_001012781.1:n.522+110G=
XR_938850.1:n.128C=
NM_000406.3:c.522+110G= MANE Select NP_000397.1:n.522+110G=
NM_001012763.2:c.522+110G= NP_001012781.1:n.522+110G=
Search 100 bp 5'
Search 100 bp 3'