Canonical Allele Identifier: CA357056204
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68619888A>C (hg19) chr4:g.67754170A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754170A>C , CM000666.2:g.67754170A>C GRCh38
NC_000004.11:g.68619888A>C , CM000666.1:g.68619888A>C GRCh37
NC_000004.10:g.68302483A>C NCBI36
NG_009293.1:g.6917T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.166T>G MANE Select ENSP00000226413.5:p.Phe56Val
ENST00000226413.4:c.166T>G ENSP00000226413.4:p.Phe56Val
ENST00000420975.2:c.166T>G ENSP00000397561.2:p.Phe56Val
NM_000406.2:c.166T>G NP_000397.1:p.Phe56Val
NM_001012763.1:c.166T>G NP_001012781.1:p.Phe56Val
NM_000406.3:c.166T>G MANE Select NP_000397.1:p.Phe56Val
NM_001012763.2:c.166T>G NP_001012781.1:p.Phe56Val
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