Canonical Allele Identifier: CA1619467767
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1788437866

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202772G>A , CM000668.2:g.32202772G>A GRCh38
NC_000006.11:g.32170549G>A , CM000668.1:g.32170549G>A GRCh37
NC_000006.10:g.32278527G>A NCBI36
NG_028190.1:g.26296C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-173C>T MANE Select ENSP00000364163.3:n.3232-173C>T
ENST00000474612.1:n.1145C>T
NM_004557.3:c.3232-173C>T NP_004548.3:n.3232-173C>T
NR_134949.1:n.3472+998C>T
NR_134950.1:n.3370+998C>T
NM_004557.4:c.3232-173C>T MANE Select NP_004548.3:n.3232-173C>T
NR_134949.2:n.3472+998C>T
NR_134950.2:n.3370+998C>T