Canonical Allele Identifier: CA1465408834
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731633148
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740278G>A , CM000666.2:g.67740278G>A GRCh38
NC_000004.11:g.68605996G>A , CM000666.1:g.68605996G>A GRCh37
NC_000004.10:g.68288591G>A NCBI36
NG_009293.1:g.20809C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*202C>T MANE Select ENSP00000226413.5:n.*202C>T
ENST00000226413.4:c.*202C>T ENSP00000226413.4:n.*202C>T
NM_000406.2:c.*202C>T NP_000397.1:n.*202C>T
NM_001012763.1:c.*311C>T NP_001012781.1:n.*311C>T
NM_000406.3:c.*202C>T MANE Select NP_000397.1:n.*202C>T
NM_001012763.2:c.*311C>T NP_001012781.1:n.*311C>T
Search 100 bp 5'
Search 100 bp 3'