Canonical Allele Identifier: CA2938919
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs750226413
ExAC: 4:68619482 A / G
gnomAD v2: 4-68619482-A-G
gnomAD v4: 4-67753764-A-G
MyVariant Identifiers: chr4:g.68619482A>G (hg19) chr4:g.67753764A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753764A>G , CM000666.2:g.67753764A>G GRCh38
NC_000004.11:g.68619482A>G , CM000666.1:g.68619482A>G GRCh37
NC_000004.10:g.68302077A>G NCBI36
NG_009293.1:g.7323T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.522+50T>C MANE Select ENSP00000226413.5:n.522+50T>C
ENST00000226413.4:c.522+50T>C ENSP00000226413.4:n.522+50T>C
ENST00000420975.2:c.522+50T>C ENSP00000397561.2:n.522+50T>C
NM_000406.2:c.522+50T>C NP_000397.1:n.522+50T>C
NM_001012763.1:c.522+50T>C NP_001012781.1:n.522+50T>C
NM_000406.3:c.522+50T>C MANE Select NP_000397.1:n.522+50T>C
NM_001012763.2:c.522+50T>C NP_001012781.1:n.522+50T>C
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