Canonical Allele Identifier: CA363557095
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs2127487341
MyVariant Identifiers: chr6:g.32188268T>C (hg19) chr6:g.32220491T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220491T>C , CM000668.2:g.32220491T>C GRCh38
NC_000006.11:g.32188268T>C , CM000668.1:g.32188268T>C GRCh37
NC_000006.10:g.32296246T>C NCBI36
NG_028190.1:g.8577A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.1073A>G MANE Select ENSP00000364163.3:p.Asp358Gly
ENST00000473562.1:n.1202A>G
NM_004557.3:c.1073A>G NP_004548.3:p.Asp358Gly
NR_134949.1:n.1212A>G
NR_134950.1:n.1212A>G
NM_004557.4:c.1073A>G MANE Select NP_004548.3:p.Asp358Gly
NR_134949.2:n.1212A>G
NR_134950.2:n.1212A>G
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