Canonical Allele Identifier: CA98667351
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs544364636
gnomAD v2: 4-68605846-C-T
gnomAD v3: 4-67740128-C-T
gnomAD v4: 4-67740128-C-T
MyVariant Identifiers: chr4:g.68605846C>T (hg19) chr4:g.67740128C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740128C>T , CM000666.2:g.67740128C>T GRCh38
NC_000004.11:g.68605846C>T , CM000666.1:g.68605846C>T GRCh37
NC_000004.10:g.68288441C>T NCBI36
NG_009293.1:g.20959G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*352G>A MANE Select ENSP00000226413.5:n.*352G>A
ENST00000226413.4:c.*352G>A ENSP00000226413.4:n.*352G>A
NM_000406.2:c.*352G>A NP_000397.1:n.*352G>A
NM_001012763.1:c.*461G>A NP_001012781.1:n.*461G>A
NM_000406.3:c.*352G>A MANE Select NP_000397.1:n.*352G>A
NM_001012763.2:c.*461G>A NP_001012781.1:n.*461G>A
Search 100 bp 5'
Search 100 bp 3'