Canonical Allele Identifier: CA98667442
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs746354614
gnomAD v2: 4-68606126-T-G
gnomAD v3: 4-67740408-T-G
gnomAD v4: 4-67740408-T-G
MyVariant Identifiers: chr4:g.68606126T>G (hg19) chr4:g.67740408T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740408T>G , CM000666.2:g.67740408T>G GRCh38
NC_000004.11:g.68606126T>G , CM000666.1:g.68606126T>G GRCh37
NC_000004.10:g.68288721T>G NCBI36
NG_009293.1:g.20679A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*72A>C MANE Select ENSP00000226413.5:n.*72A>C
ENST00000226413.4:c.*72A>C ENSP00000226413.4:n.*72A>C
NM_000406.2:c.*72A>C NP_000397.1:n.*72A>C
NM_001012763.1:c.*181A>C NP_001012781.1:n.*181A>C
NM_000406.3:c.*72A>C MANE Select NP_000397.1:n.*72A>C
NM_001012763.2:c.*181A>C NP_001012781.1:n.*181A>C
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