Canonical Allele Identifier: CA98667532
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs375002151
gnomAD v3: 4-67740573-G-A
gnomAD v4: 4-67740573-G-A
COSMIC: COSM3719147
MyVariant Identifiers: chr4:g.68606291G>A (hg19) chr4:g.67740573G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740573G>A , CM000666.2:g.67740573G>A GRCh38
NC_000004.11:g.68606291G>A , CM000666.1:g.68606291G>A GRCh37
NC_000004.10:g.68288886G>A NCBI36
NG_009293.1:g.20514C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.894C>T MANE Select ENSP00000226413.5:p.Asn298=
ENST00000226413.4:c.894C>T ENSP00000226413.4:p.Asn298=
ENST00000420975.2:c.766C>T ENSP00000397561.2:n.766C>T
NM_000406.2:c.894C>T NP_000397.1:p.Asn298=
NM_001012763.1:c.*16C>T NP_001012781.1:n.*16C>T
NM_000406.3:c.894C>T MANE Select NP_000397.1:p.Asn298=
NM_001012763.2:c.*16C>T NP_001012781.1:n.*16C>T
Search 100 bp 5'
Search 100 bp 3'