Canonical Allele Identifier: CA1344965563
Gene: JAGN1 HGNC NCBI

Linked Data

dbSNP Id: rs2082557562

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9890833A>T , CM000665.2:g.9890833A>T GRCh38
NC_000003.11:g.9932517A>T , CM000665.1:g.9932517A>T GRCh37
NC_000003.10:g.9907517A>T NCBI36
NG_041779.1:g.5247A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000489724.2:c.89+22A>T ENSP00000497724.1:n.89+22A>T
ENST00000647897.1:c.89+22A>T MANE Select ENSP00000496942.1:n.89+22A>T
ENST00000307768.4:c.89+22A>T ENSP00000306106.4:n.89+22A>T
ENST00000489724.1:n.179+22A>T
ENST00000616966.2:c.89+22A>T ENSP00000481606.1:n.89+22A>T
NM_032492.3:c.89+22A>T NP_115881.3:n.89+22A>T
NM_001363890.1:c.-180+22A>T NP_001350819.1:n.-180+22A>T
NM_032492.4:c.89+22A>T MANE Select NP_115881.3:n.89+22A>T