Canonical Allele Identifier: CA357056128
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1343752855

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754153C>G , CM000666.2:g.67754153C>G GRCh38
NC_000004.11:g.68619871C>G , CM000666.1:g.68619871C>G GRCh37
NC_000004.10:g.68302466C>G NCBI36
NG_009293.1:g.6934G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.183G>C MANE Select ENSP00000226413.5:p.Gln61His
ENST00000226413.4:c.183G>C ENSP00000226413.4:p.Gln61His
ENST00000420975.2:c.183G>C ENSP00000397561.2:p.Gln61His
NM_000406.2:c.183G>C NP_000397.1:p.Gln61His
NM_001012763.1:c.183G>C NP_001012781.1:p.Gln61His
NM_000406.3:c.183G>C MANE Select NP_000397.1:p.Gln61His
NM_001012763.2:c.183G>C NP_001012781.1:p.Gln61His