Canonical Allele Identifier: CA404513462

Gene: NOTCH3

Linked Data

• gnomAD v4: 19-15180161-G-C
• MyVariant Identifiers: chr19:g.15290972G>C (hg19) ; chr19:g.15180161G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15180161G>C , CM000681.2:g.15180161G>C	GRCh38
NC_000019.9:g.15290972G>C , CM000681.1:g.15290972G>C	GRCh37
NC_000019.8:g.15151972G>C	NCBI36
NG_009819.1:g.25821C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.3238C>G MANE Select	ENSP00000263388.1:p.His1080Asp
ENST00000263388.6:c.3238C>G	ENSP00000263388.1:p.His1080Asp
ENST00000601011.1:c.3079C>G	ENSP00000473138.1:p.His1027Asp
NM_000435.2:c.3238C>G	NP_000426.2:p.His1080Asp
XM_005259924.3:c.3082C>G	XP_005259981.1:p.His1028Asp
XM_005259924.4:c.3082C>G	XP_005259981.1:p.His1028Asp
NM_000435.3:c.3238C>G MANE Select	NP_000426.2:p.His1080Asp