Canonical Allele Identifier: CA2670820631
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754363-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754363T>C , CM000666.2:g.67754363T>C GRCh38
NC_000004.11:g.68620081T>C , CM000666.1:g.68620081T>C GRCh37
NC_000004.10:g.68302676T>C NCBI36
NG_009293.1:g.6724A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-28A>G MANE Select ENSP00000226413.5:n.-28A>G
NM_000406.2:c.-28A>G NP_000397.1:n.-28A>G
NM_001012763.1:c.-28A>G NP_001012781.1:n.-28A>G
NM_000406.3:c.-28A>G MANE Select NP_000397.1:n.-28A>G
NM_001012763.2:c.-28A>G NP_001012781.1:n.-28A>G
Search 100 bp 5'
Search 100 bp 3'