Canonical Allele Identifier: CA404533965
Gene: NOTCH3 HGNC NCBI

Linked Data

dbSNP Id: rs797045014
MyVariant Identifiers: chr19:g.15302993G>C (hg19) chr19:g.15192182G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15192182G>C , CM000681.2:g.15192182G>C GRCh38
NC_000019.9:g.15302993G>C , CM000681.1:g.15302993G>C GRCh37
NC_000019.8:g.15163993G>C NCBI36
NG_009819.1:g.13800C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263388.7:c.457C>G MANE Select ENSP00000263388.1:p.Arg153Gly
ENST00000263388.6:c.457C>G ENSP00000263388.1:p.Arg153Gly
ENST00000601011.1:c.454C>G ENSP00000473138.1:p.Arg152Gly
NM_000435.2:c.457C>G NP_000426.2:p.Arg153Gly
XM_005259924.3:c.457C>G XP_005259981.1:p.Arg153Gly
XM_005259924.4:c.457C>G XP_005259981.1:p.Arg153Gly
NM_000435.3:c.457C>G MANE Select NP_000426.2:p.Arg153Gly
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