Canonical Allele Identifier: CA305770013
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs760205888
gnomAD v2: 19-15290999-C-T
gnomAD v3: 19-15180188-C-T
gnomAD v4: 19-15180188-C-T
MyVariant Identifiers: chr19:g.15290999C>T (hg19) chr19:g.15180188C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180188C>T , CM000681.2:g.15180188C>T GRCh38
NC_000019.9:g.15290999C>T , CM000681.1:g.15290999C>T GRCh37
NC_000019.8:g.15151999C>T NCBI36
NG_009819.1:g.25794G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3211G>A MANE Select ENSP00000263388.1:p.Val1071Met
ENST00000263388.6:c.3211G>A ENSP00000263388.1:p.Val1071Met
ENST00000601011.1:c.3052G>A ENSP00000473138.1:p.Val1018Met
NM_000435.2:c.3211G>A NP_000426.2:p.Val1071Met
XM_005259924.3:c.3055G>A XP_005259981.1:p.Val1019Met
XM_005259924.4:c.3055G>A XP_005259981.1:p.Val1019Met
NM_000435.3:c.3211G>A MANE Select NP_000426.2:p.Val1071Met
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