Canonical Allele Identifier: CA2670819621
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740140-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740140G>T , CM000666.2:g.67740140G>T GRCh38
NC_000004.11:g.68605858G>T , CM000666.1:g.68605858G>T GRCh37
NC_000004.10:g.68288453G>T NCBI36
NG_009293.1:g.20947C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*340C>A MANE Select ENSP00000226413.5:n.*340C>A
ENST00000226413.4:c.*340C>A ENSP00000226413.4:n.*340C>A
NM_000406.2:c.*340C>A NP_000397.1:n.*340C>A
NM_001012763.1:c.*449C>A NP_001012781.1:n.*449C>A
NM_000406.3:c.*340C>A MANE Select NP_000397.1:n.*340C>A
NM_001012763.2:c.*449C>A NP_001012781.1:n.*449C>A
Search 100 bp 5'
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