Canonical Allele Identifier: CA420189307
Gene: NOTCH2 HGNC NCBI

Linked Data

dbSNP Id: rs1649035159
MyVariant Identifiers: chr1:g.120458181T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119915558T>C , CM000663.2:g.119915558T>C GRCh38
NC_000001.10:g.120458181T>C , CM000663.1:g.120458181T>C GRCh37
NC_000001.9:g.120259704T>C NCBI36
NG_008163.1:g.159096A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256646.7:c.7164A>G MANE Select ENSP00000256646.2:p.Ser2388=
ENST00000256646.6:c.7164A>G ENSP00000256646.2:p.Ser2388=
NM_024408.3:c.7164A>G NP_077719.2:p.Ser2388=
XM_005270901.2:c.7047A>G XP_005270958.1:p.Ser2349=
XM_011541519.1:c.7152A>G XP_011539821.1:p.Ser2384=
XM_011541520.1:c.7047A>G XP_011539822.1:p.Ser2349=
NM_024408.4:c.7164A>G MANE Select NP_077719.2:p.Ser2388=