Canonical Allele Identifier: CA2670819769

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67740429-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740429G>T , CM000666.2:g.67740429G>T	GRCh38
NC_000004.11:g.68606147G>T , CM000666.1:g.68606147G>T	GRCh37
NC_000004.10:g.68288742G>T	NCBI36
NG_009293.1:g.20658C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.*51C>A MANE Select	ENSP00000226413.5:n.*51C>A
ENST00000226413.4:c.*51C>A	ENSP00000226413.4:n.*51C>A
NM_000406.2:c.*51C>A	NP_000397.1:n.*51C>A
NM_001012763.1:c.*160C>A	NP_001012781.1:n.*160C>A
NM_000406.3:c.*51C>A MANE Select	NP_000397.1:n.*51C>A
NM_001012763.2:c.*160C>A	NP_001012781.1:n.*160C>A