Canonical Allele Identifier: CA2670819692
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740290-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740290G>T , CM000666.2:g.67740290G>T GRCh38
NC_000004.11:g.68606008G>T , CM000666.1:g.68606008G>T GRCh37
NC_000004.10:g.68288603G>T NCBI36
NG_009293.1:g.20797C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*190C>A MANE Select ENSP00000226413.5:n.*190C>A
ENST00000226413.4:c.*190C>A ENSP00000226413.4:n.*190C>A
NM_000406.2:c.*190C>A NP_000397.1:n.*190C>A
NM_001012763.1:c.*299C>A NP_001012781.1:n.*299C>A
NM_000406.3:c.*190C>A MANE Select NP_000397.1:n.*190C>A
NM_001012763.2:c.*299C>A NP_001012781.1:n.*299C>A
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