Canonical Allele Identifier: CA391271470

Gene: JAG2

Linked Data

• gnomAD v4: 14-105150714-C-G
• MyVariant Identifiers: chr14:g.105617051C>G (hg19) ; chr14:g.105150714C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105150714C>G , CM000676.2:g.105150714C>G	GRCh38
NC_000014.8:g.105617051C>G , CM000676.1:g.105617051C>G	GRCh37
NC_000014.7:g.104688096C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331782.8:c.1492G>C MANE Select	ENSP00000328169.3:p.Glu498Gln
ENST00000331782.7:c.1492G>C	ENSP00000328169.3:p.Glu498Gln
ENST00000347004.2:c.1378G>C	ENSP00000328566.2:p.Glu460Gln
NM_002226.4:c.1492G>C	NP_002217.3:p.Glu498Gln
NM_145159.2:c.1378G>C	NP_660142.1:p.Glu460Gln
XM_011536736.1:c.1492G>C	XP_011535038.1:p.Glu498Gln
XR_001750303.2:n.1553G>C
NM_002226.5:c.1492G>C MANE Select	NP_002217.3:p.Glu498Gln
NM_145159.3:c.1378G>C	NP_660142.1:p.Glu460Gln