Canonical Allele Identifier: CA357047254
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606235C>T (hg19) chr4:g.67740517C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740517C>T , CM000666.2:g.67740517C>T GRCh38
NC_000004.11:g.68606235C>T , CM000666.1:g.68606235C>T GRCh37
NC_000004.10:g.68288830C>T NCBI36
NG_009293.1:g.20570G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.950G>A MANE Select ENSP00000226413.5:p.Cys317Tyr
ENST00000226413.4:c.950G>A ENSP00000226413.4:p.Cys317Tyr
ENST00000420975.2:c.822G>A ENSP00000397561.2:n.822G>A
NM_000406.2:c.950G>A NP_000397.1:p.Cys317Tyr
NM_001012763.1:c.*72G>A NP_001012781.1:n.*72G>A
NM_000406.3:c.950G>A MANE Select NP_000397.1:p.Cys317Tyr
NM_001012763.2:c.*72G>A NP_001012781.1:n.*72G>A
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