Canonical Allele Identifier: CA9263889
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs766608781
ExAC: 19:15303034 T / A
gnomAD v2: 19-15303034-T-A
gnomAD v3: 19-15192223-T-A
gnomAD v4: 19-15192223-T-A
MyVariant Identifiers: chr19:g.15303034T>A (hg19) chr19:g.15192223T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192223T>A , CM000681.2:g.15192223T>A GRCh38
NC_000019.9:g.15303034T>A , CM000681.1:g.15303034T>A GRCh37
NC_000019.8:g.15164034T>A NCBI36
NG_009819.1:g.13759A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.416A>T MANE Select ENSP00000263388.1:p.Asp139Val
ENST00000263388.6:c.416A>T ENSP00000263388.1:p.Asp139Val
ENST00000601011.1:c.413A>T ENSP00000473138.1:p.Asp138Val
NM_000435.2:c.416A>T NP_000426.2:p.Asp139Val
XM_005259924.3:c.416A>T XP_005259981.1:p.Asp139Val
XM_005259924.4:c.416A>T XP_005259981.1:p.Asp139Val
NM_000435.3:c.416A>T MANE Select NP_000426.2:p.Asp139Val
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