Canonical Allele Identifier: CA357054316
Gene: GNRHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753834T>G , CM000666.2:g.67753834T>G GRCh38
NC_000004.11:g.68619552T>G , CM000666.1:g.68619552T>G GRCh37
NC_000004.10:g.68302147T>G NCBI36
NG_009293.1:g.7253A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.502A>C MANE Select ENSP00000226413.5:p.Ser168Arg
ENST00000226413.4:c.502A>C ENSP00000226413.4:p.Ser168Arg
ENST00000420975.2:c.502A>C ENSP00000397561.2:p.Ser168Arg
NM_000406.2:c.502A>C NP_000397.1:p.Ser168Arg
NM_001012763.1:c.502A>C NP_001012781.1:p.Ser168Arg
NM_000406.3:c.502A>C MANE Select NP_000397.1:p.Ser168Arg
NM_001012763.2:c.502A>C NP_001012781.1:p.Ser168Arg