Canonical Allele Identifier: CA2735783828
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2145432688

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187091G>A , CM000681.2:g.15187091G>A GRCh38
NC_000019.9:g.15297902G>A , CM000681.1:g.15297902G>A GRCh37
NC_000019.8:g.15158902G>A NCBI36
NG_009819.1:g.18891C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1840+14C>T MANE Select ENSP00000263388.1:n.1840+14C>T
ENST00000263388.6:c.1840+14C>T ENSP00000263388.1:n.1840+14C>T
ENST00000601011.1:c.1837+14C>T ENSP00000473138.1:n.1837+14C>T
NM_000435.2:c.1840+14C>T NP_000426.2:n.1840+14C>T
XM_005259924.3:c.1840+14C>T XP_005259981.1:n.1840+14C>T
XM_005259924.4:c.1840+14C>T XP_005259981.1:n.1840+14C>T
NM_000435.3:c.1840+14C>T MANE Select NP_000426.2:n.1840+14C>T