Canonical Allele Identifier: CA552156796
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs771419728
gnomAD v2: 4-68605995-A-G
gnomAD v3: 4-67740277-A-G
gnomAD v4: 4-67740277-A-G
MyVariant Identifiers: chr4:g.68605995A>G (hg19) chr4:g.67740277A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740277A>G , CM000666.2:g.67740277A>G GRCh38
NC_000004.11:g.68605995A>G , CM000666.1:g.68605995A>G GRCh37
NC_000004.10:g.68288590A>G NCBI36
NG_009293.1:g.20810T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*203T>C MANE Select ENSP00000226413.5:n.*203T>C
ENST00000226413.4:c.*203T>C ENSP00000226413.4:n.*203T>C
NM_000406.2:c.*203T>C NP_000397.1:n.*203T>C
NM_001012763.1:c.*312T>C NP_001012781.1:n.*312T>C
NM_000406.3:c.*203T>C MANE Select NP_000397.1:n.*203T>C
NM_001012763.2:c.*312T>C NP_001012781.1:n.*312T>C
Search 100 bp 5'
Search 100 bp 3'