Canonical Allele Identifier: CA357056273
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68619912G>T (hg19) chr4:g.67754194G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754194G>T , CM000666.2:g.67754194G>T GRCh38
NC_000004.11:g.68619912G>T , CM000666.1:g.68619912G>T GRCh37
NC_000004.10:g.68302507G>T NCBI36
NG_009293.1:g.6893C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.142C>A MANE Select ENSP00000226413.5:p.Leu48Ile
ENST00000226413.4:c.142C>A ENSP00000226413.4:p.Leu48Ile
ENST00000420975.2:c.142C>A ENSP00000397561.2:p.Leu48Ile
NM_000406.2:c.142C>A NP_000397.1:p.Leu48Ile
NM_001012763.1:c.142C>A NP_001012781.1:p.Leu48Ile
NM_000406.3:c.142C>A MANE Select NP_000397.1:p.Leu48Ile
NM_001012763.2:c.142C>A NP_001012781.1:p.Leu48Ile
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