Canonical Allele Identifier: CA439924272
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1334582087
gnomAD v2: 4-68606276-T-G
gnomAD v4: 4-67740558-T-G
MyVariant Identifiers: chr4:g.68606276T>G (hg19) chr4:g.67740558T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740558T>G , CM000666.2:g.67740558T>G GRCh38
NC_000004.11:g.68606276T>G , CM000666.1:g.68606276T>G GRCh37
NC_000004.10:g.68288871T>G NCBI36
NG_009293.1:g.20529A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.909A>C MANE Select ENSP00000226413.5:p.Pro303=
ENST00000226413.4:c.909A>C ENSP00000226413.4:p.Pro303=
ENST00000420975.2:c.781A>C ENSP00000397561.2:n.781A>C
NM_000406.2:c.909A>C NP_000397.1:p.Pro303=
NM_001012763.1:c.*31A>C NP_001012781.1:n.*31A>C
NM_000406.3:c.909A>C MANE Select NP_000397.1:p.Pro303=
NM_001012763.2:c.*31A>C NP_001012781.1:n.*31A>C
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