Canonical Allele Identifier: CA1465408975
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731636295
gnomAD v4: 4-67740437-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740437T>C , CM000666.2:g.67740437T>C GRCh38
NC_000004.11:g.68606155T>C , CM000666.1:g.68606155T>C GRCh37
NC_000004.10:g.68288750T>C NCBI36
NG_009293.1:g.20650A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*43A>G MANE Select ENSP00000226413.5:n.*43A>G
ENST00000226413.4:c.*43A>G ENSP00000226413.4:n.*43A>G
NM_000406.2:c.*43A>G NP_000397.1:n.*43A>G
NM_001012763.1:c.*152A>G NP_001012781.1:n.*152A>G
NM_000406.3:c.*43A>G MANE Select NP_000397.1:n.*43A>G
NM_001012763.2:c.*152A>G NP_001012781.1:n.*152A>G
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