Canonical Allele Identifier: CA552611477
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1170096916
gnomAD v2: 4-68620173-AC-A
gnomAD v3: 4-67754455-AC-A
gnomAD v4: 4-67754455-AC-A
MyVariant Identifiers: chr4:g.68620174del (hg19) chr4:g.67754456del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754456del , CM000666.2:g.67754456del GRCh38
NC_000004.11:g.68620174del , CM000666.1:g.68620174del GRCh37
NC_000004.10:g.68302769del NCBI36
NG_009293.1:g.6631del

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-121del NP_000397.1:n.-121del
NM_001012763.1:c.-121del NP_001012781.1:n.-121del
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