Canonical Allele Identifier: CA505827332
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2046890317
MyVariant Identifiers: chr19:g.15298085A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187274A>T , CM000681.2:g.15187274A>T GRCh38
NC_000019.9:g.15298085A>T , CM000681.1:g.15298085A>T GRCh37
NC_000019.8:g.15159085A>T NCBI36
NG_009819.1:g.18708T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1671T>A MANE Select ENSP00000263388.1:p.Gly557=
ENST00000263388.6:c.1671T>A ENSP00000263388.1:p.Gly557=
ENST00000601011.1:c.1668T>A ENSP00000473138.1:p.Gly556=
NM_000435.2:c.1671T>A NP_000426.2:p.Gly557=
XM_005259924.3:c.1671T>A XP_005259981.1:p.Gly557=
XM_005259924.4:c.1671T>A XP_005259981.1:p.Gly557=
NM_000435.3:c.1671T>A MANE Select NP_000426.2:p.Gly557=
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