Canonical Allele Identifier: CA2670819763
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740423-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740423G>T , CM000666.2:g.67740423G>T GRCh38
NC_000004.11:g.68606141G>T , CM000666.1:g.68606141G>T GRCh37
NC_000004.10:g.68288736G>T NCBI36
NG_009293.1:g.20664C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*57C>A MANE Select ENSP00000226413.5:n.*57C>A
ENST00000226413.4:c.*57C>A ENSP00000226413.4:n.*57C>A
NM_000406.2:c.*57C>A NP_000397.1:n.*57C>A
NM_001012763.1:c.*166C>A NP_001012781.1:n.*166C>A
NM_000406.3:c.*57C>A MANE Select NP_000397.1:n.*57C>A
NM_001012763.2:c.*166C>A NP_001012781.1:n.*166C>A
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