Canonical Allele Identifier: CA341877614

Gene: NOTCH2

Linked Data

• dbSNP Id: rs2101143707
• MyVariant Identifiers: chr1:g.120510083C>G (hg19) ; chr1:g.119967460C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119967460C>G , CM000663.2:g.119967460C>G	GRCh38
NC_000001.10:g.120510083C>G , CM000663.1:g.120510083C>G	GRCh37
NC_000001.9:g.120311606C>G	NCBI36
NG_008163.1:g.107194G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000256646.7:c.1426G>C MANE Select	ENSP00000256646.2:p.Gly476Arg
ENST00000640021.1:c.646G>C	ENSP00000492223.1:n.646G>C
ENST00000256646.6:c.1426G>C	ENSP00000256646.2:p.Gly476Arg
ENST00000479412.2:n.1564G>C
ENST00000579475.7:c.1309G>C	ENSP00000477065.2:p.Gly437Arg
NM_001200001.1:c.1426G>C	NP_001186930.1:p.Gly476Arg
NM_024408.3:c.1426G>C	NP_077719.2:p.Gly476Arg
XM_005270901.2:c.1309G>C	XP_005270958.1:p.Gly437Arg
XM_011541519.1:c.1414G>C	XP_011539821.1:p.Gly472Arg
XM_011541520.1:c.1309G>C	XP_011539822.1:p.Gly437Arg
NM_024408.4:c.1426G>C MANE Select	NP_077719.2:p.Gly476Arg
NM_001200001.2:c.1426G>C	NP_001186930.1:p.Gly476Arg