Canonical Allele Identifier: CA357047584
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1275111761
gnomAD v2: 4-68606306-A-T
gnomAD v4: 4-67740588-A-T
MyVariant Identifiers: chr4:g.68606306A>T (hg19) chr4:g.67740588A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740588A>T , CM000666.2:g.67740588A>T GRCh38
NC_000004.11:g.68606306A>T , CM000666.1:g.68606306A>T GRCh37
NC_000004.10:g.68288901A>T NCBI36
NG_009293.1:g.20499T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.879T>A MANE Select ENSP00000226413.5:p.Asp293Glu
ENST00000226413.4:c.879T>A ENSP00000226413.4:p.Asp293Glu
ENST00000420975.2:c.751T>A ENSP00000397561.2:n.751T>A
NM_000406.2:c.879T>A NP_000397.1:p.Asp293Glu
NM_001012763.1:c.*1T>A NP_001012781.1:n.*1T>A
NM_000406.3:c.879T>A MANE Select NP_000397.1:p.Asp293Glu
NM_001012763.2:c.*1T>A NP_001012781.1:n.*1T>A
Search 100 bp 5'
Search 100 bp 3'