Canonical Allele Identifier: CA2938856
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs778297307
ExAC: 4:68606420 C / T
gnomAD v2: 4-68606420-C-T
gnomAD v4: 4-67740702-C-T
MyVariant Identifiers: chr4:g.68606420C>T (hg19) chr4:g.67740702C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740702C>T , CM000666.2:g.67740702C>T GRCh38
NC_000004.11:g.68606420C>T , CM000666.1:g.68606420C>T GRCh37
NC_000004.10:g.68289015C>T NCBI36
NG_009293.1:g.20385G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.765G>A MANE Select ENSP00000226413.5:p.Lys255=
ENST00000226413.4:c.765G>A ENSP00000226413.4:p.Lys255=
ENST00000420975.2:c.637G>A ENSP00000397561.2:p.Glu213Lys
NM_000406.2:c.765G>A NP_000397.1:p.Lys255=
NM_001012763.1:c.637G>A NP_001012781.1:p.Glu213Lys
NM_000406.3:c.765G>A MANE Select NP_000397.1:p.Lys255=
NM_001012763.2:c.637G>A NP_001012781.1:p.Glu213Lys
Search 100 bp 5'
Search 100 bp 3'