Canonical Allele Identifier: CA439924385
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731640048
gnomAD v4: 4-67740597-A-G
MyVariant Identifiers: chr4:g.68606315A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740597A>G , CM000666.2:g.67740597A>G GRCh38
NC_000004.11:g.68606315A>G , CM000666.1:g.68606315A>G GRCh37
NC_000004.10:g.68288910A>G NCBI36
NG_009293.1:g.20490T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.870T>C MANE Select ENSP00000226413.5:p.Tyr290=
ENST00000226413.4:c.870T>C ENSP00000226413.4:p.Tyr290=
ENST00000420975.2:c.742T>C ENSP00000397561.2:p.Leu248=
NM_000406.2:c.870T>C NP_000397.1:p.Tyr290=
NM_001012763.1:c.742T>C NP_001012781.1:p.Leu248=
NM_000406.3:c.870T>C MANE Select NP_000397.1:p.Tyr290=
NM_001012763.2:c.742T>C NP_001012781.1:p.Leu248=
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