Canonical Allele Identifier: CA505824418
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs752588207
MyVariant Identifiers: chr19:g.15291036A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180225A>T , CM000681.2:g.15180225A>T GRCh38
NC_000019.9:g.15291036A>T , CM000681.1:g.15291036A>T GRCh37
NC_000019.8:g.15152036A>T NCBI36
NG_009819.1:g.25757T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.3174T>A MANE Select ENSP00000263388.1:p.Gly1058=
ENST00000263388.6:c.3174T>A ENSP00000263388.1:p.Gly1058=
ENST00000601011.1:c.3015T>A ENSP00000473138.1:p.Gly1005=
NM_000435.2:c.3174T>A NP_000426.2:p.Gly1058=
XM_005259924.3:c.3018T>A XP_005259981.1:p.Gly1006=
XM_005259924.4:c.3018T>A XP_005259981.1:p.Gly1006=
NM_000435.3:c.3174T>A MANE Select NP_000426.2:p.Gly1058=