Canonical Allele Identifier: CA2670819594

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67740083-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740083C>A , CM000666.2:g.67740083C>A	GRCh38
NC_000004.11:g.68605801C>A , CM000666.1:g.68605801C>A	GRCh37
NC_000004.10:g.68288396C>A	NCBI36
NG_009293.1:g.21004G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*397G>T MANE Select	ENSP00000226413.5:n.*397G>T
ENST00000226413.4:c.*397G>T	ENSP00000226413.4:n.*397G>T
NM_000406.2:c.*397G>T	NP_000397.1:n.*397G>T
NM_001012763.1:c.*506G>T	NP_001012781.1:n.*506G>T
NM_000406.3:c.*397G>T MANE Select	NP_000397.1:n.*397G>T
NM_001012763.2:c.*506G>T	NP_001012781.1:n.*506G>T