Canonical Allele Identifier: CA2939018
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs762299416
ExAC: 4:68620050 C / T
gnomAD v2: 4-68620050-C-T
COSMIC: COSM5060429
MyVariant Identifiers: chr4:g.68620050C>T (hg19) chr4:g.67754332C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754332C>T , CM000666.2:g.67754332C>T GRCh38
NC_000004.11:g.68620050C>T , CM000666.1:g.68620050C>T GRCh37
NC_000004.10:g.68302645C>T NCBI36
NG_009293.1:g.6755G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.4G>A MANE Select ENSP00000226413.5:p.Ala2Thr
ENST00000226413.4:c.4G>A ENSP00000226413.4:p.Ala2Thr
ENST00000420975.2:c.4G>A ENSP00000397561.2:p.Ala2Thr
NM_000406.2:c.4G>A NP_000397.1:p.Ala2Thr
NM_001012763.1:c.4G>A NP_001012781.1:p.Ala2Thr
NM_000406.3:c.4G>A MANE Select NP_000397.1:p.Ala2Thr
NM_001012763.2:c.4G>A NP_001012781.1:p.Ala2Thr
Search 100 bp 5'
Search 100 bp 3'