Canonical Allele Identifier: CA2938851
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs542566291
ExAC: 4:68606378 C / T
gnomAD v2: 4-68606378-C-T
gnomAD v3: 4-67740660-C-T
gnomAD v4: 4-67740660-C-T
MyVariant Identifiers: chr4:g.68606378C>T (hg19) chr4:g.67740660C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740660C>T , CM000666.2:g.67740660C>T GRCh38
NC_000004.11:g.68606378C>T , CM000666.1:g.68606378C>T GRCh37
NC_000004.10:g.68288973C>T NCBI36
NG_009293.1:g.20427G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.807G>A MANE Select ENSP00000226413.5:p.Thr269=
ENST00000226413.4:c.807G>A ENSP00000226413.4:p.Thr269=
ENST00000420975.2:c.679G>A ENSP00000397561.2:p.Gly227Ser
NM_000406.2:c.807G>A NP_000397.1:p.Thr269=
NM_001012763.1:c.679G>A NP_001012781.1:p.Gly227Ser
NM_000406.3:c.807G>A MANE Select NP_000397.1:p.Thr269=
NM_001012763.2:c.679G>A NP_001012781.1:p.Gly227Ser
Search 100 bp 5'
Search 100 bp 3'