Canonical Allele Identifier: CA488731447
Gene: JAG2 HGNC NCBI

Linked Data

gnomAD v4: 14-105150718-C-T
MyVariant Identifiers: chr14:g.105617055C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105150718C>T , CM000676.2:g.105150718C>T GRCh38
NC_000014.8:g.105617055C>T , CM000676.1:g.105617055C>T GRCh37
NC_000014.7:g.104688100C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331782.8:c.1488G>A MANE Select ENSP00000328169.3:p.Glu496=
ENST00000331782.7:c.1488G>A ENSP00000328169.3:p.Glu496=
ENST00000347004.2:c.1374G>A ENSP00000328566.2:p.Glu458=
NM_002226.4:c.1488G>A NP_002217.3:p.Glu496=
NM_145159.2:c.1374G>A NP_660142.1:p.Glu458=
XM_011536736.1:c.1488G>A XP_011535038.1:p.Glu496=
XR_001750303.2:n.1549G>A
NM_002226.5:c.1488G>A MANE Select NP_002217.3:p.Glu496=
NM_145159.3:c.1374G>A NP_660142.1:p.Glu458=
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Search 100 bp 3'