Canonical Allele Identifier: CA357047619
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606311A>G (hg19) chr4:g.67740593A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740593A>G , CM000666.2:g.67740593A>G GRCh38
NC_000004.11:g.68606311A>G , CM000666.1:g.68606311A>G GRCh37
NC_000004.10:g.68288906A>G NCBI36
NG_009293.1:g.20494T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.874T>C MANE Select ENSP00000226413.5:p.Phe292Leu
ENST00000226413.4:c.874T>C ENSP00000226413.4:p.Phe292Leu
ENST00000420975.2:c.746T>C ENSP00000397561.2:p.Val249Ala
NM_000406.2:c.874T>C NP_000397.1:p.Phe292Leu
NM_001012763.1:c.746T>C NP_001012781.1:p.Val249Ala
NM_000406.3:c.874T>C MANE Select NP_000397.1:p.Phe292Leu
NM_001012763.2:c.746T>C NP_001012781.1:p.Val249Ala
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