Canonical Allele Identifier: CA2670819706
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740320-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740320T>C , CM000666.2:g.67740320T>C GRCh38
NC_000004.11:g.68606038T>C , CM000666.1:g.68606038T>C GRCh37
NC_000004.10:g.68288633T>C NCBI36
NG_009293.1:g.20767A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*160A>G MANE Select ENSP00000226413.5:n.*160A>G
ENST00000226413.4:c.*160A>G ENSP00000226413.4:n.*160A>G
NM_000406.2:c.*160A>G NP_000397.1:n.*160A>G
NM_001012763.1:c.*269A>G NP_001012781.1:n.*269A>G
NM_000406.3:c.*160A>G MANE Select NP_000397.1:n.*160A>G
NM_001012763.2:c.*269A>G NP_001012781.1:n.*269A>G