Canonical Allele Identifier: CA357047758
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606333A>T (hg19) chr4:g.67740615A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740615A>T , CM000666.2:g.67740615A>T GRCh38
NC_000004.11:g.68606333A>T , CM000666.1:g.68606333A>T GRCh37
NC_000004.10:g.68288928A>T NCBI36
NG_009293.1:g.20472T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.852T>A MANE Select ENSP00000226413.5:p.Tyr284Ter
ENST00000226413.4:c.852T>A ENSP00000226413.4:p.Tyr284Ter
ENST00000420975.2:c.724T>A ENSP00000397561.2:p.Cys242Ser
NM_000406.2:c.852T>A NP_000397.1:p.Tyr284Ter
NM_001012763.1:c.724T>A NP_001012781.1:p.Cys242Ser
NM_000406.3:c.852T>A MANE Select NP_000397.1:p.Tyr284Ter
NM_001012763.2:c.724T>A NP_001012781.1:p.Cys242Ser
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