Canonical Allele Identifier: CA2670820689
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754476-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754476T>A , CM000666.2:g.67754476T>A GRCh38
NC_000004.11:g.68620194T>A , CM000666.1:g.68620194T>A GRCh37
NC_000004.10:g.68302789T>A NCBI36
NG_009293.1:g.6611A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-141A>T NP_000397.1:n.-141A>T
NM_001012763.1:c.-141A>T NP_001012781.1:n.-141A>T