Canonical Allele Identifier: CA1465421102
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731934529
gnomAD v4: 4-67754491-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754491G>T , CM000666.2:g.67754491G>T GRCh38
NC_000004.11:g.68620209G>T , CM000666.1:g.68620209G>T GRCh37
NC_000004.10:g.68302804G>T NCBI36
NG_009293.1:g.6596C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-156C>A NP_000397.1:n.-156C>A
NM_001012763.1:c.-156C>A NP_001012781.1:n.-156C>A