Canonical Allele Identifier: CA2735671481
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs2046826095
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15180036A>T , CM000681.2:g.15180036A>T GRCh38
NC_000019.9:g.15290847A>T , CM000681.1:g.15290847A>T GRCh37
NC_000019.8:g.15151847A>T NCBI36
NG_009819.1:g.25946T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.3327+36T>A MANE Select ENSP00000263388.1:n.3327+36T>A
ENST00000263388.6:c.3327+36T>A ENSP00000263388.1:n.3327+36T>A
ENST00000601011.1:c.3168+36T>A ENSP00000473138.1:n.3168+36T>A
NM_000435.2:c.3327+36T>A NP_000426.2:n.3327+36T>A
XM_005259924.3:c.3171+36T>A XP_005259981.1:n.3171+36T>A
XM_005259924.4:c.3171+36T>A XP_005259981.1:n.3171+36T>A
NM_000435.3:c.3327+36T>A MANE Select NP_000426.2:n.3327+36T>A
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