Canonical Allele Identifier: CA2670819619
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740138-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740138T>C , CM000666.2:g.67740138T>C GRCh38
NC_000004.11:g.68605856T>C , CM000666.1:g.68605856T>C GRCh37
NC_000004.10:g.68288451T>C NCBI36
NG_009293.1:g.20949A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*342A>G MANE Select ENSP00000226413.5:n.*342A>G
ENST00000226413.4:c.*342A>G ENSP00000226413.4:n.*342A>G
NM_000406.2:c.*342A>G NP_000397.1:n.*342A>G
NM_001012763.1:c.*451A>G NP_001012781.1:n.*451A>G
NM_000406.3:c.*342A>G MANE Select NP_000397.1:n.*342A>G
NM_001012763.2:c.*451A>G NP_001012781.1:n.*451A>G