Canonical Allele Identifier: CA797693210
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1471290730
gnomAD v3: 4-67740101-G-C
gnomAD v4: 4-67740101-G-C
MyVariant Identifiers: chr4:g.68605819G>C (hg19) chr4:g.67740101G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740101G>C , CM000666.2:g.67740101G>C GRCh38
NC_000004.11:g.68605819G>C , CM000666.1:g.68605819G>C GRCh37
NC_000004.10:g.68288414G>C NCBI36
NG_009293.1:g.20986C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*379C>G MANE Select ENSP00000226413.5:n.*379C>G
ENST00000226413.4:c.*379C>G ENSP00000226413.4:n.*379C>G
NM_000406.2:c.*379C>G NP_000397.1:n.*379C>G
NM_001012763.1:c.*488C>G NP_001012781.1:n.*488C>G
NM_000406.3:c.*379C>G MANE Select NP_000397.1:n.*379C>G
NM_001012763.2:c.*488C>G NP_001012781.1:n.*488C>G
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