Canonical Allele Identifier: CA1465408960

Gene: GNRHR

Linked Data

• dbSNP Id: rs1577865738
• gnomAD v4: 4-67740420-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740420C>A , CM000666.2:g.67740420C>A	GRCh38
NC_000004.11:g.68606138C>A , CM000666.1:g.68606138C>A	GRCh37
NC_000004.10:g.68288733C>A	NCBI36
NG_009293.1:g.20667G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*60G>T MANE Select	ENSP00000226413.5:n.*60G>T
ENST00000226413.4:c.*60G>T	ENSP00000226413.4:n.*60G>T
NM_000406.2:c.*60G>T	NP_000397.1:n.*60G>T
NM_001012763.1:c.*169G>T	NP_001012781.1:n.*169G>T
NM_000406.3:c.*60G>T MANE Select	NP_000397.1:n.*60G>T
NM_001012763.2:c.*169G>T	NP_001012781.1:n.*169G>T