Canonical Allele Identifier: CA2705810324

Gene: GNRHR

Linked Data

• dbSNP Id: rs1224982943

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740342T>C , CM000666.2:g.67740342T>C	GRCh38
NC_000004.11:g.68606060T>C , CM000666.1:g.68606060T>C	GRCh37
NC_000004.10:g.68288655T>C	NCBI36
NG_009293.1:g.20745A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.*138A>G MANE Select	ENSP00000226413.5:n.*138A>G
ENST00000226413.4:c.*138A>G	ENSP00000226413.4:n.*138A>G
NM_000406.2:c.*138A>G	NP_000397.1:n.*138A>G
NM_001012763.1:c.*247A>G	NP_001012781.1:n.*247A>G
NM_000406.3:c.*138A>G MANE Select	NP_000397.1:n.*138A>G
NM_001012763.2:c.*247A>G	NP_001012781.1:n.*247A>G