Canonical Allele Identifier: CA2670819766
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740428-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740428A>C , CM000666.2:g.67740428A>C GRCh38
NC_000004.11:g.68606146A>C , CM000666.1:g.68606146A>C GRCh37
NC_000004.10:g.68288741A>C NCBI36
NG_009293.1:g.20659T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*52T>G MANE Select ENSP00000226413.5:n.*52T>G
ENST00000226413.4:c.*52T>G ENSP00000226413.4:n.*52T>G
NM_000406.2:c.*52T>G NP_000397.1:n.*52T>G
NM_001012763.1:c.*161T>G NP_001012781.1:n.*161T>G
NM_000406.3:c.*52T>G MANE Select NP_000397.1:n.*52T>G
NM_001012763.2:c.*161T>G NP_001012781.1:n.*161T>G