Canonical Allele Identifier: CA357048603
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606444T>A (hg19) chr4:g.67740726T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740726T>A , CM000666.2:g.67740726T>A GRCh38
NC_000004.11:g.68606444T>A , CM000666.1:g.68606444T>A GRCh37
NC_000004.10:g.68289039T>A NCBI36
NG_009293.1:g.20361A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.743-2A>T MANE Select ENSP00000226413.5:n.743-2A>T
ENST00000226413.4:c.743-2A>T ENSP00000226413.4:n.743-2A>T
ENST00000420975.2:c.615-2A>T ENSP00000397561.2:n.615-2A>T
NM_000406.2:c.743-2A>T NP_000397.1:n.743-2A>T
NM_001012763.1:c.615-2A>T NP_001012781.1:n.615-2A>T
NM_000406.3:c.743-2A>T MANE Select NP_000397.1:n.743-2A>T
NM_001012763.2:c.615-2A>T NP_001012781.1:n.615-2A>T
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