Canonical Allele Identifier: CA357048337
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1221081120
gnomAD v2: 4-68606402-T-A
gnomAD v4: 4-67740684-T-A
MyVariant Identifiers: chr4:g.68606402T>A (hg19) chr4:g.67740684T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.783A>T MANE Select ENSP00000226413.5:p.Ala261=
ENST00000226413.4:c.783A>T ENSP00000226413.4:p.Ala261=
ENST00000420975.2:c.655A>T ENSP00000397561.2:p.Thr219Ser
NM_000406.2:c.783A>T NP_000397.1:p.Ala261=
NM_001012763.1:c.655A>T NP_001012781.1:p.Thr219Ser
NM_000406.3:c.783A>T MANE Select NP_000397.1:p.Ala261=
NM_001012763.2:c.655A>T NP_001012781.1:p.Thr219Ser
Search 100 bp 5'
Search 100 bp 3'