Canonical Allele Identifier: CA2670819629

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67740150-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740150T>A , CM000666.2:g.67740150T>A	GRCh38
NC_000004.11:g.68605868T>A , CM000666.1:g.68605868T>A	GRCh37
NC_000004.10:g.68288463T>A	NCBI36
NG_009293.1:g.20937A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*330A>T MANE Select	ENSP00000226413.5:n.*330A>T
ENST00000226413.4:c.*330A>T	ENSP00000226413.4:n.*330A>T
NM_000406.2:c.*330A>T	NP_000397.1:n.*330A>T
NM_001012763.1:c.*439A>T	NP_001012781.1:n.*439A>T
NM_000406.3:c.*330A>T MANE Select	NP_000397.1:n.*330A>T
NM_001012763.2:c.*439A>T	NP_001012781.1:n.*439A>T