Canonical Allele Identifier: CA305769878
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs947008097
MyVariant Identifiers: chr19:g.15290743A>G (hg19) chr19:g.15179932A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15179932A>G , CM000681.2:g.15179932A>G GRCh38
NC_000019.9:g.15290743A>G , CM000681.1:g.15290743A>G GRCh37
NC_000019.8:g.15151743A>G NCBI36
NG_009819.1:g.26050T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3327+140T>C MANE Select ENSP00000263388.1:n.3327+140T>C
ENST00000263388.6:c.3327+140T>C ENSP00000263388.1:n.3327+140T>C
ENST00000601011.1:c.3168+140T>C ENSP00000473138.1:n.3168+140T>C
NM_000435.2:c.3327+140T>C NP_000426.2:n.3327+140T>C
XM_005259924.3:c.3171+140T>C XP_005259981.1:n.3171+140T>C
XM_005259924.4:c.3171+140T>C XP_005259981.1:n.3171+140T>C
NM_000435.3:c.3327+140T>C MANE Select NP_000426.2:n.3327+140T>C
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