Canonical Allele Identifier: CA2706125270

Gene: GNRHR

Linked Data

• dbSNP Id: rs2109981374

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740732A>C , CM000666.2:g.67740732A>C	GRCh38
NC_000004.11:g.68606450A>C , CM000666.1:g.68606450A>C	GRCh37
NC_000004.10:g.68289045A>C	NCBI36
NG_009293.1:g.20355T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.743-8T>G MANE Select	ENSP00000226413.5:n.743-8T>G
ENST00000226413.4:c.743-8T>G	ENSP00000226413.4:n.743-8T>G
ENST00000420975.2:c.615-8T>G	ENSP00000397561.2:n.615-8T>G
NM_000406.2:c.743-8T>G	NP_000397.1:n.743-8T>G
NM_001012763.1:c.615-8T>G	NP_001012781.1:n.615-8T>G
NM_000406.3:c.743-8T>G MANE Select	NP_000397.1:n.743-8T>G
NM_001012763.2:c.615-8T>G	NP_001012781.1:n.615-8T>G