Canonical Allele Identifier: CA305770161
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs899284827
MyVariant Identifiers: chr19:g.15291339T>C (hg19) chr19:g.15180528T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180528T>C , CM000681.2:g.15180528T>C GRCh38
NC_000019.9:g.15291339T>C , CM000681.1:g.15291339T>C GRCh37
NC_000019.8:g.15152339T>C NCBI36
NG_009819.1:g.25454A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3142+153A>G MANE Select ENSP00000263388.1:n.3142+153A>G
ENST00000263388.6:c.3142+153A>G ENSP00000263388.1:n.3142+153A>G
ENST00000601011.1:c.2983+153A>G ENSP00000473138.1:n.2983+153A>G
NM_000435.2:c.3142+153A>G NP_000426.2:n.3142+153A>G
XM_005259924.3:c.2986+153A>G XP_005259981.1:n.2986+153A>G
XM_005259924.4:c.2986+153A>G XP_005259981.1:n.2986+153A>G
NM_000435.3:c.3142+153A>G MANE Select NP_000426.2:n.3142+153A>G
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