Canonical Allele Identifier: CA404513832
Gene: NOTCH3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.15291028C>G (hg19) chr19:g.15180217C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180217C>G , CM000681.2:g.15180217C>G GRCh38
NC_000019.9:g.15291028C>G , CM000681.1:g.15291028C>G GRCh37
NC_000019.8:g.15152028C>G NCBI36
NG_009819.1:g.25765G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.3182G>C MANE Select ENSP00000263388.1:p.Cys1061Ser
ENST00000263388.6:c.3182G>C ENSP00000263388.1:p.Cys1061Ser
ENST00000601011.1:c.3023G>C ENSP00000473138.1:p.Cys1008Ser
NM_000435.2:c.3182G>C NP_000426.2:p.Cys1061Ser
XM_005259924.3:c.3026G>C XP_005259981.1:p.Cys1009Ser
XM_005259924.4:c.3026G>C XP_005259981.1:p.Cys1009Ser
NM_000435.3:c.3182G>C MANE Select NP_000426.2:p.Cys1061Ser
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