Canonical Allele Identifier: CA1465421032
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731931570

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754363del , CM000666.2:g.67754363del GRCh38
NC_000004.11:g.68620081del , CM000666.1:g.68620081del GRCh37
NC_000004.10:g.68302676del NCBI36
NG_009293.1:g.6725del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-27del MANE Select ENSP00000226413.5:n.-27del
NM_000406.2:c.-27del NP_000397.1:n.-27del
NM_001012763.1:c.-27del NP_001012781.1:n.-27del
NM_000406.3:c.-27del MANE Select NP_000397.1:n.-27del
NM_001012763.2:c.-27del NP_001012781.1:n.-27del