Canonical Allele Identifier: CA2583063802
Gene: NOTCH3 HGNC NCBI

Linked Data

gnomAD v4: 19-15184202-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15184202A>G , CM000681.2:g.15184202A>G GRCh38
NC_000019.9:g.15295013A>G , CM000681.1:g.15295013A>G GRCh37
NC_000019.8:g.15156013A>G NCBI36
NG_009819.1:g.21780T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.2566+93T>C MANE Select ENSP00000263388.1:n.2566+93T>C
ENST00000263388.6:c.2566+93T>C ENSP00000263388.1:n.2566+93T>C
ENST00000601011.1:c.2407+704T>C ENSP00000473138.1:n.2407+704T>C
NM_000435.2:c.2566+93T>C NP_000426.2:n.2566+93T>C
XM_005259924.3:c.2410+704T>C XP_005259981.1:n.2410+704T>C
XM_005259924.4:c.2410+704T>C XP_005259981.1:n.2410+704T>C
NM_000435.3:c.2566+93T>C MANE Select NP_000426.2:n.2566+93T>C
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