Canonical Allele Identifier: CA632128095
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs1272414564
gnomAD v2: 19-15302542-G-C
gnomAD v4: 19-15191731-G-C
MyVariant Identifiers: chr19:g.15302542G>C (hg19) chr19:g.15191731G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15191731G>C , CM000681.2:g.15191731G>C GRCh38
NC_000019.9:g.15302542G>C , CM000681.1:g.15302542G>C GRCh37
NC_000019.8:g.15163542G>C NCBI36
NG_009819.1:g.14251C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.802+14C>G MANE Select ENSP00000263388.1:n.802+14C>G
ENST00000263388.6:c.802+14C>G ENSP00000263388.1:n.802+14C>G
ENST00000601011.1:c.799+14C>G ENSP00000473138.1:n.799+14C>G
NM_000435.2:c.802+14C>G NP_000426.2:n.802+14C>G
XM_005259924.3:c.802+14C>G XP_005259981.1:n.802+14C>G
XM_005259924.4:c.802+14C>G XP_005259981.1:n.802+14C>G
NM_000435.3:c.802+14C>G MANE Select NP_000426.2:n.802+14C>G
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