Canonical Allele Identifier: CA1465408709
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731629884
gnomAD v4: 4-67740141-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740141G>T , CM000666.2:g.67740141G>T GRCh38
NC_000004.11:g.68605859G>T , CM000666.1:g.68605859G>T GRCh37
NC_000004.10:g.68288454G>T NCBI36
NG_009293.1:g.20946C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*339C>A MANE Select ENSP00000226413.5:n.*339C>A
ENST00000226413.4:c.*339C>A ENSP00000226413.4:n.*339C>A
NM_000406.2:c.*339C>A NP_000397.1:n.*339C>A
NM_001012763.1:c.*448C>A NP_001012781.1:n.*448C>A
NM_000406.3:c.*339C>A MANE Select NP_000397.1:n.*339C>A
NM_001012763.2:c.*448C>A NP_001012781.1:n.*448C>A
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