Canonical Allele Identifier: CA439928838
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1560520046
gnomAD v4: 4-67753826-A-G
MyVariant Identifiers: chr4:g.68619544A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753826A>G , CM000666.2:g.67753826A>G GRCh38
NC_000004.11:g.68619544A>G , CM000666.1:g.68619544A>G GRCh37
NC_000004.10:g.68302139A>G NCBI36
NG_009293.1:g.7261T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.510T>C MANE Select ENSP00000226413.5:p.Phe170=
ENST00000226413.4:c.510T>C ENSP00000226413.4:p.Phe170=
ENST00000420975.2:c.510T>C ENSP00000397561.2:p.Phe170=
NM_000406.2:c.510T>C NP_000397.1:p.Phe170=
NM_001012763.1:c.510T>C NP_001012781.1:p.Phe170=
NM_000406.3:c.510T>C MANE Select NP_000397.1:p.Phe170=
NM_001012763.2:c.510T>C NP_001012781.1:p.Phe170=
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