Canonical Allele Identifier: CA9263832
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs764093604
ExAC: 19:15302781 G / C
gnomAD v2: 19-15302781-G-C
gnomAD v4: 19-15191970-G-C
MyVariant Identifiers: chr19:g.15302781G>C (hg19) chr19:g.15191970G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191970G>C , CM000681.2:g.15191970G>C GRCh38
NC_000019.9:g.15302781G>C , CM000681.1:g.15302781G>C GRCh37
NC_000019.8:g.15163781G>C NCBI36
NG_009819.1:g.14012C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.669C>G MANE Select ENSP00000263388.1:p.Ala223=
ENST00000263388.6:c.669C>G ENSP00000263388.1:p.Ala223=
ENST00000601011.1:c.666C>G ENSP00000473138.1:p.Ala222=
NM_000435.2:c.669C>G NP_000426.2:p.Ala223=
XM_005259924.3:c.669C>G XP_005259981.1:p.Ala223=
XM_005259924.4:c.669C>G XP_005259981.1:p.Ala223=
NM_000435.3:c.669C>G MANE Select NP_000426.2:p.Ala223=
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