Canonical Allele Identifier: CA432386350
Gene: JAGN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.9932466G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9890782G>T , CM000665.2:g.9890782G>T GRCh38
NC_000003.11:g.9932466G>T , CM000665.1:g.9932466G>T GRCh37
NC_000003.10:g.9907466G>T NCBI36
NG_041779.1:g.5196G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000489724.2:c.60G>T ENSP00000497724.1:p.Arg20=
ENST00000647897.1:c.60G>T MANE Select ENSP00000496942.1:p.Arg20=
ENST00000307768.4:c.60G>T ENSP00000306106.4:p.Arg20=
ENST00000489724.1:n.150G>T
ENST00000616966.2:c.60G>T ENSP00000481606.1:p.Arg20=
NM_032492.3:c.60G>T NP_115881.3:p.Arg20=
NM_001363890.1:c.-209G>T NP_001350819.1:n.-209G>T
NM_032492.4:c.60G>T MANE Select NP_115881.3:p.Arg20=