Canonical Allele Identifier: CA1465421099
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754490T= , CM000666.2:g.67754490T= GRCh38
NC_000004.11:g.68620208T= , CM000666.1:g.68620208T= GRCh37
NC_000004.10:g.68302803T= NCBI36
NG_009293.1:g.6597A=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-155A= NP_000397.1:n.-155A=
NM_001012763.1:c.-155A= NP_001012781.1:n.-155A=