Canonical Allele Identifier: CA506078618
Gene: NOTCH3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15302784A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191973A>G , CM000681.2:g.15191973A>G GRCh38
NC_000019.9:g.15302784A>G , CM000681.1:g.15302784A>G GRCh37
NC_000019.8:g.15163784A>G NCBI36
NG_009819.1:g.14009T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.666T>C MANE Select ENSP00000263388.1:p.Cys222=
ENST00000263388.6:c.666T>C ENSP00000263388.1:p.Cys222=
ENST00000601011.1:c.663T>C ENSP00000473138.1:p.Cys221=
NM_000435.2:c.666T>C NP_000426.2:p.Cys222=
XM_005259924.3:c.666T>C XP_005259981.1:p.Cys222=
XM_005259924.4:c.666T>C XP_005259981.1:p.Cys222=
NM_000435.3:c.666T>C MANE Select NP_000426.2:p.Cys222=
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