Canonical Allele Identifier: CA30309355

Gene: NOTCH2

Linked Data

• dbSNP Id: rs1040526755
• gnomAD v3: 1-119975386-G-A
• gnomAD v4: 1-119975386-G-A
• MyVariant Identifiers: chr1:g.119975386G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119975386G>A , CM000663.2:g.119975386G>A	GRCh38
NC_000001.10:g.120518009G>A , CM000663.1:g.120518009G>A	GRCh37
NC_000001.9:g.120319532G>A	NCBI36
NG_008163.1:g.99268C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000256646.7:c.875-5642C>T MANE Select	ENSP00000256646.2:n.875-5642C>T
ENST00000640021.1:c.94+964C>T	ENSP00000492223.1:n.94+964C>T
ENST00000256646.6:c.875-5642C>T	ENSP00000256646.2:n.875-5642C>T
ENST00000479412.2:n.1013-5642C>T
ENST00000579475.7:c.758-5642C>T	ENSP00000477065.2:n.758-5642C>T
NM_001200001.1:c.875-5642C>T	NP_001186930.1:n.875-5642C>T
NM_024408.3:c.875-5642C>T	NP_077719.2:n.875-5642C>T
XM_005270901.2:c.758-5642C>T	XP_005270958.1:n.758-5642C>T
XM_011541519.1:c.863-5642C>T	XP_011539821.1:n.863-5642C>T
XM_011541520.1:c.758-5642C>T	XP_011539822.1:n.758-5642C>T
NM_024408.4:c.875-5642C>T MANE Select	NP_077719.2:n.875-5642C>T
NM_001200001.2:c.875-5642C>T	NP_001186930.1:n.875-5642C>T