Canonical Allele Identifier: CA797693216

Gene: GNRHR

Linked Data

• dbSNP Id: rs1481586728
• MyVariant Identifiers: chr4:g.68605834G>A (hg19) ; chr4:g.67740116G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740116G>A , CM000666.2:g.67740116G>A	GRCh38
NC_000004.11:g.68605834G>A , CM000666.1:g.68605834G>A	GRCh37
NC_000004.10:g.68288429G>A	NCBI36
NG_009293.1:g.20971C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*364C>T MANE Select	ENSP00000226413.5:n.*364C>T
ENST00000226413.4:c.*364C>T	ENSP00000226413.4:n.*364C>T
NM_000406.2:c.*364C>T	NP_000397.1:n.*364C>T
NM_001012763.1:c.*473C>T	NP_001012781.1:n.*473C>T
NM_000406.3:c.*364C>T MANE Select	NP_000397.1:n.*364C>T
NM_001012763.2:c.*473C>T	NP_001012781.1:n.*473C>T