Canonical Allele Identifier: CA2670819772
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740431-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740431G>T , CM000666.2:g.67740431G>T GRCh38
NC_000004.11:g.68606149G>T , CM000666.1:g.68606149G>T GRCh37
NC_000004.10:g.68288744G>T NCBI36
NG_009293.1:g.20656C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*49C>A MANE Select ENSP00000226413.5:n.*49C>A
ENST00000226413.4:c.*49C>A ENSP00000226413.4:n.*49C>A
NM_000406.2:c.*49C>A NP_000397.1:n.*49C>A
NM_001012763.1:c.*158C>A NP_001012781.1:n.*158C>A
NM_000406.3:c.*49C>A MANE Select NP_000397.1:n.*49C>A
NM_001012763.2:c.*158C>A NP_001012781.1:n.*158C>A
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