Canonical Allele Identifier: CA136901388

Gene: NOTCH4

Linked Data

• dbSNP Id: rs1051721921
• MyVariant Identifiers: chr6:g.32173040T>C (hg19) ; chr6:g.32205263T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32205263T>C , CM000668.2:g.32205263T>C	GRCh38
NC_000006.11:g.32173040T>C , CM000668.1:g.32173040T>C	GRCh37
NC_000006.10:g.32281018T>C	NCBI36
NG_028190.1:g.23805A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375023.3:c.2866-874A>G MANE Select	ENSP00000364163.3:n.2866-874A>G
NM_004557.3:c.2866-874A>G	NP_004548.3:n.2866-874A>G
NR_134949.1:n.3107-874A>G
NR_134950.1:n.3005-874A>G
NM_004557.4:c.2866-874A>G MANE Select	NP_004548.3:n.2866-874A>G
NR_134949.2:n.3107-874A>G
NR_134950.2:n.3005-874A>G