Canonical Allele Identifier: CA2670819813
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740732-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740732A>T , CM000666.2:g.67740732A>T GRCh38
NC_000004.11:g.68606450A>T , CM000666.1:g.68606450A>T GRCh37
NC_000004.10:g.68289045A>T NCBI36
NG_009293.1:g.20355T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.743-8T>A MANE Select ENSP00000226413.5:n.743-8T>A
ENST00000226413.4:c.743-8T>A ENSP00000226413.4:n.743-8T>A
ENST00000420975.2:c.615-8T>A ENSP00000397561.2:n.615-8T>A
NM_000406.2:c.743-8T>A NP_000397.1:n.743-8T>A
NM_001012763.1:c.615-8T>A NP_001012781.1:n.615-8T>A
NM_000406.3:c.743-8T>A MANE Select NP_000397.1:n.743-8T>A
NM_001012763.2:c.615-8T>A NP_001012781.1:n.615-8T>A
Search 100 bp 5'
Search 100 bp 3'