Canonical Allele Identifier: CA2670819722
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740349-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740349G>A , CM000666.2:g.67740349G>A GRCh38
NC_000004.11:g.68606067G>A , CM000666.1:g.68606067G>A GRCh37
NC_000004.10:g.68288662G>A NCBI36
NG_009293.1:g.20738C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*131C>T MANE Select ENSP00000226413.5:n.*131C>T
ENST00000226413.4:c.*131C>T ENSP00000226413.4:n.*131C>T
NM_000406.2:c.*131C>T NP_000397.1:n.*131C>T
NM_001012763.1:c.*240C>T NP_001012781.1:n.*240C>T
NM_000406.3:c.*131C>T MANE Select NP_000397.1:n.*131C>T
NM_001012763.2:c.*240C>T NP_001012781.1:n.*240C>T