Canonical Allele Identifier: CA2938945
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs780544773
ExAC: 4:68619651 T / C
gnomAD v2: 4-68619651-T-C
gnomAD v4: 4-67753933-T-C
MyVariant Identifiers: chr4:g.68619651T>C (hg19) chr4:g.67753933T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753933T>C , CM000666.2:g.67753933T>C GRCh38
NC_000004.11:g.68619651T>C , CM000666.1:g.68619651T>C GRCh37
NC_000004.10:g.68302246T>C NCBI36
NG_009293.1:g.7154A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.403A>G MANE Select ENSP00000226413.5:p.Ile135Val
ENST00000226413.4:c.403A>G ENSP00000226413.4:p.Ile135Val
ENST00000420975.2:c.403A>G ENSP00000397561.2:p.Ile135Val
NM_000406.2:c.403A>G NP_000397.1:p.Ile135Val
NM_001012763.1:c.403A>G NP_001012781.1:p.Ile135Val
NM_000406.3:c.403A>G MANE Select NP_000397.1:p.Ile135Val
NM_001012763.2:c.403A>G NP_001012781.1:p.Ile135Val
Search 100 bp 5'
Search 100 bp 3'