Canonical Allele Identifier: CA404533911
Gene: NOTCH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192167C>A , CM000681.2:g.15192167C>A GRCh38
NC_000019.9:g.15302978C>A , CM000681.1:g.15302978C>A GRCh37
NC_000019.8:g.15163978C>A NCBI36
NG_009819.1:g.13815G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.472G>T MANE Select ENSP00000263388.1:p.Asp158Tyr
ENST00000263388.6:c.472G>T ENSP00000263388.1:p.Asp158Tyr
ENST00000601011.1:c.469G>T ENSP00000473138.1:p.Asp157Tyr
NM_000435.2:c.472G>T NP_000426.2:p.Asp158Tyr
XM_005259924.3:c.472G>T XP_005259981.1:p.Asp158Tyr
XM_005259924.4:c.472G>T XP_005259981.1:p.Asp158Tyr
NM_000435.3:c.472G>T MANE Select NP_000426.2:p.Asp158Tyr