Canonical Allele Identifier: CA552611447
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1380596095
gnomAD v2: 4-68606161-T-A
gnomAD v3: 4-67740443-T-A
gnomAD v4: 4-67740443-T-A
MyVariant Identifiers: chr4:g.68606161T>A (hg19) chr4:g.67740443T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740443T>A , CM000666.2:g.67740443T>A GRCh38
NC_000004.11:g.68606161T>A , CM000666.1:g.68606161T>A GRCh37
NC_000004.10:g.68288756T>A NCBI36
NG_009293.1:g.20644A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*37A>T MANE Select ENSP00000226413.5:n.*37A>T
ENST00000226413.4:c.*37A>T ENSP00000226413.4:n.*37A>T
NM_000406.2:c.*37A>T NP_000397.1:n.*37A>T
NM_001012763.1:c.*146A>T NP_001012781.1:n.*146A>T
NM_000406.3:c.*37A>T MANE Select NP_000397.1:n.*37A>T
NM_001012763.2:c.*146A>T NP_001012781.1:n.*146A>T
Search 100 bp 5'
Search 100 bp 3'