Canonical Allele Identifier: CA357047408
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740547-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740547A>G , CM000666.2:g.67740547A>G GRCh38
NC_000004.11:g.68606265A>G , CM000666.1:g.68606265A>G GRCh37
NC_000004.10:g.68288860A>G NCBI36
NG_009293.1:g.20540T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.920T>C MANE Select ENSP00000226413.5:p.Phe307Ser
ENST00000226413.4:c.920T>C ENSP00000226413.4:p.Phe307Ser
ENST00000420975.2:c.792T>C ENSP00000397561.2:n.792T>C
NM_000406.2:c.920T>C NP_000397.1:p.Phe307Ser
NM_001012763.1:c.*42T>C NP_001012781.1:n.*42T>C
NM_000406.3:c.920T>C MANE Select NP_000397.1:p.Phe307Ser
NM_001012763.2:c.*42T>C NP_001012781.1:n.*42T>C