Canonical Allele Identifier: CA506078814
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2145441825
gnomAD v4: 19-15192123-G-A
MyVariant Identifiers: chr19:g.15302934G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192123G>A , CM000681.2:g.15192123G>A GRCh38
NC_000019.9:g.15302934G>A , CM000681.1:g.15302934G>A GRCh37
NC_000019.8:g.15163934G>A NCBI36
NG_009819.1:g.13859C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.516C>T MANE Select ENSP00000263388.1:p.Gly172=
ENST00000263388.6:c.516C>T ENSP00000263388.1:p.Gly172=
ENST00000601011.1:c.513C>T ENSP00000473138.1:p.Gly171=
NM_000435.2:c.516C>T NP_000426.2:p.Gly172=
XM_005259924.3:c.516C>T XP_005259981.1:p.Gly172=
XM_005259924.4:c.516C>T XP_005259981.1:p.Gly172=
NM_000435.3:c.516C>T MANE Select NP_000426.2:p.Gly172=
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