Canonical Allele Identifier: CA1465420339
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731912162
gnomAD v4: 4-67753729-A-ACTTC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753733_67753736dup , CM000666.2:g.67753733_67753736dup GRCh38
NC_000004.11:g.68619451_68619454dup , CM000666.1:g.68619451_68619454dup GRCh37
NC_000004.10:g.68302046_68302049dup NCBI36
NG_009293.1:g.7354_7357dup

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.522+81_522+84dup MANE Select ENSP00000226413.5:n.522+81_522+84dup
ENST00000226413.4:c.522+81_522+84dup ENSP00000226413.4:n.522+81_522+84dup
ENST00000420975.2:c.522+81_522+84dup ENSP00000397561.2:n.522+81_522+84dup
NM_000406.2:c.522+81_522+84dup NP_000397.1:n.522+81_522+84dup
NM_001012763.1:c.522+81_522+84dup NP_001012781.1:n.522+81_522+84dup
NM_000406.3:c.522+81_522+84dup MANE Select NP_000397.1:n.522+81_522+84dup
NM_001012763.2:c.522+81_522+84dup NP_001012781.1:n.522+81_522+84dup
Search 100 bp 5'
Search 100 bp 3'