Canonical Allele Identifier: CA357048339
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 717649
ClinVar RCV Id: RCV000890475
dbSNP Id: rs1221081120
MyVariant Identifiers: chr4:g.68606402T>C (hg19) chr4:g.67740684T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740684T>C , CM000666.2:g.67740684T>C GRCh38
NC_000004.11:g.68606402T>C , CM000666.1:g.68606402T>C GRCh37
NC_000004.10:g.68288997T>C NCBI36
NG_009293.1:g.20403A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.783A>G MANE Select ENSP00000226413.5:p.Ala261=
ENST00000226413.4:c.783A>G ENSP00000226413.4:p.Ala261=
ENST00000420975.2:c.655A>G ENSP00000397561.2:p.Thr219Ala
NM_000406.2:c.783A>G NP_000397.1:p.Ala261=
NM_001012763.1:c.655A>G NP_001012781.1:p.Thr219Ala
NM_000406.3:c.783A>G MANE Select NP_000397.1:p.Ala261=
NM_001012763.2:c.655A>G NP_001012781.1:p.Thr219Ala
Search 100 bp 5'
Search 100 bp 3'