Canonical Allele Identifier: CA404524152
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs753801611
gnomAD v2: 19-15297737-G-C
gnomAD v3: 19-15186926-G-C
gnomAD v4: 19-15186926-G-C
MyVariant Identifiers: chr19:g.15297737G>C (hg19) chr19:g.15186926G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15186926G>C , CM000681.2:g.15186926G>C GRCh38
NC_000019.9:g.15297737G>C , CM000681.1:g.15297737G>C GRCh37
NC_000019.8:g.15158737G>C NCBI36
NG_009819.1:g.19056C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1903C>G MANE Select ENSP00000263388.1:p.Arg635Gly
ENST00000263388.6:c.1903C>G ENSP00000263388.1:p.Arg635Gly
ENST00000601011.1:c.1900C>G ENSP00000473138.1:p.Arg634Gly
NM_000435.2:c.1903C>G NP_000426.2:p.Arg635Gly
XM_005259924.3:c.1903C>G XP_005259981.1:p.Arg635Gly
XM_005259924.4:c.1903C>G XP_005259981.1:p.Arg635Gly
NM_000435.3:c.1903C>G MANE Select NP_000426.2:p.Arg635Gly
Search 100 bp 5'
Search 100 bp 3'