Canonical Allele Identifier: CA2578100630
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740408-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740408T>C , CM000666.2:g.67740408T>C GRCh38
NC_000004.11:g.68606126T>C , CM000666.1:g.68606126T>C GRCh37
NC_000004.10:g.68288721T>C NCBI36
NG_009293.1:g.20679A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*72A>G MANE Select ENSP00000226413.5:n.*72A>G
ENST00000226413.4:c.*72A>G ENSP00000226413.4:n.*72A>G
NM_000406.2:c.*72A>G NP_000397.1:n.*72A>G
NM_001012763.1:c.*181A>G NP_001012781.1:n.*181A>G
NM_000406.3:c.*72A>G MANE Select NP_000397.1:n.*72A>G
NM_001012763.2:c.*181A>G NP_001012781.1:n.*181A>G