Canonical Allele Identifier: CA341878407

Gene: NOTCH2

Linked Data

• MyVariant Identifiers: chr1:g.120510203T>C (hg19) ; chr1:g.119967580T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119967580T>C , CM000663.2:g.119967580T>C	GRCh38
NC_000001.10:g.120510203T>C , CM000663.1:g.120510203T>C	GRCh37
NC_000001.9:g.120311726T>C	NCBI36
NG_008163.1:g.107074A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256646.7:c.1306A>G MANE Select	ENSP00000256646.2:p.Thr436Ala
ENST00000640021.1:c.526A>G	ENSP00000492223.1:n.526A>G
ENST00000256646.6:c.1306A>G	ENSP00000256646.2:p.Thr436Ala
ENST00000479412.2:n.1444A>G
ENST00000579475.7:c.1189A>G	ENSP00000477065.2:p.Thr397Ala
NM_001200001.1:c.1306A>G	NP_001186930.1:p.Thr436Ala
NM_024408.3:c.1306A>G	NP_077719.2:p.Thr436Ala
XM_005270901.2:c.1189A>G	XP_005270958.1:p.Thr397Ala
XM_011541519.1:c.1294A>G	XP_011539821.1:p.Thr432Ala
XM_011541520.1:c.1189A>G	XP_011539822.1:p.Thr397Ala
NM_024408.4:c.1306A>G MANE Select	NP_077719.2:p.Thr436Ala
NM_001200001.2:c.1306A>G	NP_001186930.1:p.Thr436Ala