Canonical Allele Identifier: CA98667416
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs528918332
gnomAD v2: 4-68606039-T-C
gnomAD v3: 4-67740321-T-C
gnomAD v4: 4-67740321-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740321T>C , CM000666.2:g.67740321T>C GRCh38
NC_000004.11:g.68606039T>C , CM000666.1:g.68606039T>C GRCh37
NC_000004.10:g.68288634T>C NCBI36
NG_009293.1:g.20766A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*159A>G MANE Select ENSP00000226413.5:n.*159A>G
ENST00000226413.4:c.*159A>G ENSP00000226413.4:n.*159A>G
NM_000406.2:c.*159A>G NP_000397.1:n.*159A>G
NM_001012763.1:c.*268A>G NP_001012781.1:n.*268A>G
NM_000406.3:c.*159A>G MANE Select NP_000397.1:n.*159A>G
NM_001012763.2:c.*268A>G NP_001012781.1:n.*268A>G