Canonical Allele Identifier: CA98667408
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs566335091
gnomAD v2: 4-68606009-T-A
gnomAD v3: 4-67740291-T-A
gnomAD v4: 4-67740291-T-A
MyVariant Identifiers: chr4:g.68606009T>A (hg19) chr4:g.67740291T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740291T>A , CM000666.2:g.67740291T>A GRCh38
NC_000004.11:g.68606009T>A , CM000666.1:g.68606009T>A GRCh37
NC_000004.10:g.68288604T>A NCBI36
NG_009293.1:g.20796A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*189A>T MANE Select ENSP00000226413.5:n.*189A>T
ENST00000226413.4:c.*189A>T ENSP00000226413.4:n.*189A>T
NM_000406.2:c.*189A>T NP_000397.1:n.*189A>T
NM_001012763.1:c.*298A>T NP_001012781.1:n.*298A>T
NM_000406.3:c.*189A>T MANE Select NP_000397.1:n.*189A>T
NM_001012763.2:c.*298A>T NP_001012781.1:n.*298A>T
Search 100 bp 5'
Search 100 bp 3'