Canonical Allele Identifier: CA2670819600

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67740092-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740092G>A , CM000666.2:g.67740092G>A	GRCh38
NC_000004.11:g.68605810G>A , CM000666.1:g.68605810G>A	GRCh37
NC_000004.10:g.68288405G>A	NCBI36
NG_009293.1:g.20995C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*388C>T MANE Select	ENSP00000226413.5:n.*388C>T
ENST00000226413.4:c.*388C>T	ENSP00000226413.4:n.*388C>T
NM_000406.2:c.*388C>T	NP_000397.1:n.*388C>T
NM_001012763.1:c.*497C>T	NP_001012781.1:n.*497C>T
NM_000406.3:c.*388C>T MANE Select	NP_000397.1:n.*388C>T
NM_001012763.2:c.*497C>T	NP_001012781.1:n.*497C>T