Canonical Allele Identifier: CA404533192

Gene: NOTCH3

Linked Data

• MyVariant Identifiers: chr19:g.15302811C>G (hg19) ; chr19:g.15192000C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15192000C>G , CM000681.2:g.15192000C>G	GRCh38
NC_000019.9:g.15302811C>G , CM000681.1:g.15302811C>G	GRCh37
NC_000019.8:g.15163811C>G	NCBI36
NG_009819.1:g.13982G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263388.7:c.639G>C MANE Select	ENSP00000263388.1:p.Arg213Ser
ENST00000263388.6:c.639G>C	ENSP00000263388.1:p.Arg213Ser
ENST00000601011.1:c.636G>C	ENSP00000473138.1:p.Arg212Ser
NM_000435.2:c.639G>C	NP_000426.2:p.Arg213Ser
XM_005259924.3:c.639G>C	XP_005259981.1:p.Arg213Ser
XM_005259924.4:c.639G>C	XP_005259981.1:p.Arg213Ser
NM_000435.3:c.639G>C MANE Select	NP_000426.2:p.Arg213Ser