Canonical Allele Identifier: CA439924251
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606273T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740555T>C , CM000666.2:g.67740555T>C GRCh38
NC_000004.11:g.68606273T>C , CM000666.1:g.68606273T>C GRCh37
NC_000004.10:g.68288868T>C NCBI36
NG_009293.1:g.20532A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.912A>G MANE Select ENSP00000226413.5:p.Val304=
ENST00000226413.4:c.912A>G ENSP00000226413.4:p.Val304=
ENST00000420975.2:c.784A>G ENSP00000397561.2:n.784A>G
NM_000406.2:c.912A>G NP_000397.1:p.Val304=
NM_001012763.1:c.*34A>G NP_001012781.1:n.*34A>G
NM_000406.3:c.912A>G MANE Select NP_000397.1:p.Val304=
NM_001012763.2:c.*34A>G NP_001012781.1:n.*34A>G
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