Canonical Allele Identifier: CA2670819714
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740334-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740334A>T , CM000666.2:g.67740334A>T GRCh38
NC_000004.11:g.68606052A>T , CM000666.1:g.68606052A>T GRCh37
NC_000004.10:g.68288647A>T NCBI36
NG_009293.1:g.20753T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*146T>A MANE Select ENSP00000226413.5:n.*146T>A
ENST00000226413.4:c.*146T>A ENSP00000226413.4:n.*146T>A
NM_000406.2:c.*146T>A NP_000397.1:n.*146T>A
NM_001012763.1:c.*255T>A NP_001012781.1:n.*255T>A
NM_000406.3:c.*146T>A MANE Select NP_000397.1:n.*146T>A
NM_001012763.2:c.*255T>A NP_001012781.1:n.*255T>A
Search 100 bp 5'
Search 100 bp 3'