Canonical Allele Identifier: CA506078433
Gene: NOTCH3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15297953C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187142C>A , CM000681.2:g.15187142C>A GRCh38
NC_000019.9:g.15297953C>A , CM000681.1:g.15297953C>A GRCh37
NC_000019.8:g.15158953C>A NCBI36
NG_009819.1:g.18840G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1803G>T MANE Select ENSP00000263388.1:p.Val601=
ENST00000263388.6:c.1803G>T ENSP00000263388.1:p.Val601=
ENST00000601011.1:c.1800G>T ENSP00000473138.1:p.Val600=
NM_000435.2:c.1803G>T NP_000426.2:p.Val601=
XM_005259924.3:c.1803G>T XP_005259981.1:p.Val601=
XM_005259924.4:c.1803G>T XP_005259981.1:p.Val601=
NM_000435.3:c.1803G>T MANE Select NP_000426.2:p.Val601=
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