Canonical Allele Identifier: CA305774710

Gene: NOTCH3

Linked Data

• dbSNP Id: rs764263853
• gnomAD v4: 19-15186985-A-G
• MyVariant Identifiers: chr19:g.15297796A>G (hg19) ; chr19:g.15186985A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15186985A>G , CM000681.2:g.15186985A>G	GRCh38
NC_000019.9:g.15297796A>G , CM000681.1:g.15297796A>G	GRCh37
NC_000019.8:g.15158796A>G	NCBI36
NG_009819.1:g.18997T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.1844T>C MANE Select	ENSP00000263388.1:p.Val615Ala
ENST00000263388.6:c.1844T>C	ENSP00000263388.1:p.Val615Ala
ENST00000601011.1:c.1841T>C	ENSP00000473138.1:p.Val614Ala
NM_000435.2:c.1844T>C	NP_000426.2:p.Val615Ala
XM_005259924.3:c.1844T>C	XP_005259981.1:p.Val615Ala
XM_005259924.4:c.1844T>C	XP_005259981.1:p.Val615Ala
NM_000435.3:c.1844T>C MANE Select	NP_000426.2:p.Val615Ala