Canonical Allele Identifier: CA2670819661
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740219-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740219A>G , CM000666.2:g.67740219A>G GRCh38
NC_000004.11:g.68605937A>G , CM000666.1:g.68605937A>G GRCh37
NC_000004.10:g.68288532A>G NCBI36
NG_009293.1:g.20868T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*261T>C MANE Select ENSP00000226413.5:n.*261T>C
ENST00000226413.4:c.*261T>C ENSP00000226413.4:n.*261T>C
NM_000406.2:c.*261T>C NP_000397.1:n.*261T>C
NM_001012763.1:c.*370T>C NP_001012781.1:n.*370T>C
NM_000406.3:c.*261T>C MANE Select NP_000397.1:n.*261T>C
NM_001012763.2:c.*370T>C NP_001012781.1:n.*370T>C
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