Canonical Allele Identifier: CA357047777
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606336G>T (hg19) chr4:g.67740618G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740618G>T , CM000666.2:g.67740618G>T GRCh38
NC_000004.11:g.68606336G>T , CM000666.1:g.68606336G>T GRCh37
NC_000004.10:g.68288931G>T NCBI36
NG_009293.1:g.20469C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.849C>A MANE Select ENSP00000226413.5:p.Tyr283Ter
ENST00000226413.4:c.849C>A ENSP00000226413.4:p.Tyr283Ter
ENST00000420975.2:c.721C>A ENSP00000397561.2:p.Leu241Ile
NM_000406.2:c.849C>A NP_000397.1:p.Tyr283Ter
NM_001012763.1:c.721C>A NP_001012781.1:p.Leu241Ile
NM_000406.3:c.849C>A MANE Select NP_000397.1:p.Tyr283Ter
NM_001012763.2:c.721C>A NP_001012781.1:p.Leu241Ile
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