Canonical Allele Identifier: CA2324749946
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192003G= , CM000681.2:g.15192003G= GRCh38
NC_000019.9:g.15302814G= , CM000681.1:g.15302814G= GRCh37
NC_000019.8:g.15163814G= NCBI36
NG_009819.1:g.13979C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.636C= MANE Select ENSP00000263388.1:p.Cys212=
ENST00000263388.6:c.636C= ENSP00000263388.1:p.Cys212=
ENST00000601011.1:c.633C= ENSP00000473138.1:p.Cys211=
NM_000435.2:c.636C= NP_000426.2:p.Cys212=
XM_005259924.3:c.636C= XP_005259981.1:p.Cys212=
XM_005259924.4:c.636C= XP_005259981.1:p.Cys212=
NM_000435.3:c.636C= MANE Select NP_000426.2:p.Cys212=