Canonical Allele Identifier: CA2670819657
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740214-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740214C>A , CM000666.2:g.67740214C>A GRCh38
NC_000004.11:g.68605932C>A , CM000666.1:g.68605932C>A GRCh37
NC_000004.10:g.68288527C>A NCBI36
NG_009293.1:g.20873G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*266G>T MANE Select ENSP00000226413.5:n.*266G>T
ENST00000226413.4:c.*266G>T ENSP00000226413.4:n.*266G>T
NM_000406.2:c.*266G>T NP_000397.1:n.*266G>T
NM_001012763.1:c.*375G>T NP_001012781.1:n.*375G>T
NM_000406.3:c.*266G>T MANE Select NP_000397.1:n.*266G>T
NM_001012763.2:c.*375G>T NP_001012781.1:n.*375G>T
Search 100 bp 5'
Search 100 bp 3'