Canonical Allele Identifier: CA357054343
Gene: GNRHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753846A>T , CM000666.2:g.67753846A>T GRCh38
NC_000004.11:g.68619564A>T , CM000666.1:g.68619564A>T GRCh37
NC_000004.10:g.68302159A>T NCBI36
NG_009293.1:g.7241T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.490T>A MANE Select ENSP00000226413.5:p.Trp164Arg
ENST00000226413.4:c.490T>A ENSP00000226413.4:p.Trp164Arg
ENST00000420975.2:c.490T>A ENSP00000397561.2:p.Trp164Arg
NM_000406.2:c.490T>A NP_000397.1:p.Trp164Arg
NM_001012763.1:c.490T>A NP_001012781.1:p.Trp164Arg
NM_000406.3:c.490T>A MANE Select NP_000397.1:p.Trp164Arg
NM_001012763.2:c.490T>A NP_001012781.1:p.Trp164Arg