Canonical Allele Identifier: CA1063692887
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731634357
gnomAD v3: 4-67740352-T-A
gnomAD v4: 4-67740352-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740352T>A , CM000666.2:g.67740352T>A GRCh38
NC_000004.11:g.68606070T>A , CM000666.1:g.68606070T>A GRCh37
NC_000004.10:g.68288665T>A NCBI36
NG_009293.1:g.20735A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*128A>T MANE Select ENSP00000226413.5:n.*128A>T
ENST00000226413.4:c.*128A>T ENSP00000226413.4:n.*128A>T
NM_000406.2:c.*128A>T NP_000397.1:n.*128A>T
NM_001012763.1:c.*237A>T NP_001012781.1:n.*237A>T
NM_000406.3:c.*128A>T MANE Select NP_000397.1:n.*128A>T
NM_001012763.2:c.*237A>T NP_001012781.1:n.*237A>T
Search 100 bp 5'
Search 100 bp 3'