Canonical Allele Identifier: CA2324750035
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192187T= , CM000681.2:g.15192187T= GRCh38
NC_000019.9:g.15302998T= , CM000681.1:g.15302998T= GRCh37
NC_000019.8:g.15163998T= NCBI36
NG_009819.1:g.13795A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.452A= MANE Select ENSP00000263388.1:p.Gln151=
ENST00000263388.6:c.452A= ENSP00000263388.1:p.Gln151=
ENST00000601011.1:c.449A= ENSP00000473138.1:p.Gln150=
NM_000435.2:c.452A= NP_000426.2:p.Gln151=
XM_005259924.3:c.452A= XP_005259981.1:p.Gln151=
XM_005259924.4:c.452A= XP_005259981.1:p.Gln151=
NM_000435.3:c.452A= MANE Select NP_000426.2:p.Gln151=