Canonical Allele Identifier: CA391271463

Gene: JAG2

Linked Data

• gnomAD v4: 14-105150711-G-A
• COSMIC: COSM4645179
• MyVariant Identifiers: chr14:g.105617048G>A (hg19) ; chr14:g.105150711G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105150711G>A , CM000676.2:g.105150711G>A	GRCh38
NC_000014.8:g.105617048G>A , CM000676.1:g.105617048G>A	GRCh37
NC_000014.7:g.104688093G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331782.8:c.1495C>T MANE Select	ENSP00000328169.3:p.Arg499Ter
ENST00000331782.7:c.1495C>T	ENSP00000328169.3:p.Arg499Ter
ENST00000347004.2:c.1381C>T	ENSP00000328566.2:p.Arg461Ter
NM_002226.4:c.1495C>T	NP_002217.3:p.Arg499Ter
NM_145159.2:c.1381C>T	NP_660142.1:p.Arg461Ter
XM_011536736.1:c.1495C>T	XP_011535038.1:p.Arg499Ter
XR_001750303.2:n.1556C>T
NM_002226.5:c.1495C>T MANE Select	NP_002217.3:p.Arg499Ter
NM_145159.3:c.1381C>T	NP_660142.1:p.Arg461Ter