Canonical Allele Identifier: CA506078867
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2145442015
MyVariant Identifiers: chr19:g.15302970A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192159A>G , CM000681.2:g.15192159A>G GRCh38
NC_000019.9:g.15302970A>G , CM000681.1:g.15302970A>G GRCh37
NC_000019.8:g.15163970A>G NCBI36
NG_009819.1:g.13823T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.480T>C MANE Select ENSP00000263388.1:p.Asp160=
ENST00000263388.6:c.480T>C ENSP00000263388.1:p.Asp160=
ENST00000601011.1:c.477T>C ENSP00000473138.1:p.Asp159=
NM_000435.2:c.480T>C NP_000426.2:p.Asp160=
XM_005259924.3:c.480T>C XP_005259981.1:p.Asp160=
XM_005259924.4:c.480T>C XP_005259981.1:p.Asp160=
NM_000435.3:c.480T>C MANE Select NP_000426.2:p.Asp160=
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