Canonical Allele Identifier: CA404533848
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1599394895

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192148A>C , CM000681.2:g.15192148A>C GRCh38
NC_000019.9:g.15302959A>C , CM000681.1:g.15302959A>C GRCh37
NC_000019.8:g.15163959A>C NCBI36
NG_009819.1:g.13834T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.491T>G MANE Select ENSP00000263388.1:p.Val164Gly
ENST00000263388.6:c.491T>G ENSP00000263388.1:p.Val164Gly
ENST00000601011.1:c.488T>G ENSP00000473138.1:p.Val163Gly
NM_000435.2:c.491T>G NP_000426.2:p.Val164Gly
XM_005259924.3:c.491T>G XP_005259981.1:p.Val164Gly
XM_005259924.4:c.491T>G XP_005259981.1:p.Val164Gly
NM_000435.3:c.491T>G MANE Select NP_000426.2:p.Val164Gly