Canonical Allele Identifier: CA9263842
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs777092861
ExAC: 19:15302815 C / T
gnomAD v2: 19-15302815-C-T
MyVariant Identifiers: chr19:g.15302815C>T (hg19) chr19:g.15192004C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192004C>T , CM000681.2:g.15192004C>T GRCh38
NC_000019.9:g.15302815C>T , CM000681.1:g.15302815C>T GRCh37
NC_000019.8:g.15163815C>T NCBI36
NG_009819.1:g.13978G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.635G>A MANE Select ENSP00000263388.1:p.Cys212Tyr
ENST00000263388.6:c.635G>A ENSP00000263388.1:p.Cys212Tyr
ENST00000601011.1:c.632G>A ENSP00000473138.1:p.Cys211Tyr
NM_000435.2:c.635G>A NP_000426.2:p.Cys212Tyr
XM_005259924.3:c.635G>A XP_005259981.1:p.Cys212Tyr
XM_005259924.4:c.635G>A XP_005259981.1:p.Cys212Tyr
NM_000435.3:c.635G>A MANE Select NP_000426.2:p.Cys212Tyr
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