Canonical Allele Identifier: CA2670820619
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754336-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754340del , CM000666.2:g.67754340del GRCh38
NC_000004.11:g.68620058del , CM000666.1:g.68620058del GRCh37
NC_000004.10:g.68302653del NCBI36
NG_009293.1:g.6750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-2del MANE Select ENSP00000226413.5:n.-2del
ENST00000226413.4:c.-2del ENSP00000226413.4:n.-2del
NM_000406.2:c.-2del NP_000397.1:n.-2del
NM_001012763.1:c.-2del NP_001012781.1:n.-2del
NM_000406.3:c.-2del MANE Select NP_000397.1:n.-2del
NM_001012763.2:c.-2del NP_001012781.1:n.-2del
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