Canonical Allele Identifier: CA357054597
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1428587227
gnomAD v2: 4-68619650-A-T
gnomAD v4: 4-67753932-A-T
MyVariant Identifiers: chr4:g.68619650A>T (hg19) chr4:g.67753932A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753932A>T , CM000666.2:g.67753932A>T GRCh38
NC_000004.11:g.68619650A>T , CM000666.1:g.68619650A>T GRCh37
NC_000004.10:g.68302245A>T NCBI36
NG_009293.1:g.7155T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.404T>A MANE Select ENSP00000226413.5:p.Ile135Asn
ENST00000226413.4:c.404T>A ENSP00000226413.4:p.Ile135Asn
ENST00000420975.2:c.404T>A ENSP00000397561.2:p.Ile135Asn
NM_000406.2:c.404T>A NP_000397.1:p.Ile135Asn
NM_001012763.1:c.404T>A NP_001012781.1:p.Ile135Asn
NM_000406.3:c.404T>A MANE Select NP_000397.1:p.Ile135Asn
NM_001012763.2:c.404T>A NP_001012781.1:p.Ile135Asn
Search 100 bp 5'
Search 100 bp 3'