Canonical Allele Identifier: CA2670819617
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740130-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740130T>G , CM000666.2:g.67740130T>G GRCh38
NC_000004.11:g.68605848T>G , CM000666.1:g.68605848T>G GRCh37
NC_000004.10:g.68288443T>G NCBI36
NG_009293.1:g.20957A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*350A>C MANE Select ENSP00000226413.5:n.*350A>C
ENST00000226413.4:c.*350A>C ENSP00000226413.4:n.*350A>C
NM_000406.2:c.*350A>C NP_000397.1:n.*350A>C
NM_001012763.1:c.*459A>C NP_001012781.1:n.*459A>C
NM_000406.3:c.*350A>C MANE Select NP_000397.1:n.*350A>C
NM_001012763.2:c.*459A>C NP_001012781.1:n.*459A>C
Search 100 bp 5'
Search 100 bp 3'