Canonical Allele Identifier: CA914360025
Gene: NBAS HGNC NCBI

Linked Data

dbSNP Id: rs1558325804
gnomAD v2: 2-15564751-C-A
gnomAD v3: 2-15424627-C-A
gnomAD v4: 2-15424627-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424627C>A , CM000664.2:g.15424627C>A GRCh38
NC_000002.11:g.15564751C>A , CM000664.1:g.15564751C>A GRCh37
NC_000002.10:g.15482202C>A NCBI36
NG_032964.1:g.141722G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.521-159G>T
ENST00000700062.1:c.521-159G>T
ENST00000700065.1:n.2437-159G>T
ENST00000700066.1:c.1941-159G>T ENSP00000514780.1:n.1941-159G>T
ENST00000281513.10:c.2424-159G>T MANE Select ENSP00000281513.5:n.2424-159G>T
ENST00000281513.9:c.2424-159G>T ENSP00000281513.5:n.2424-159G>T
NM_015909.3:c.2424-159G>T NP_056993.2:n.2424-159G>T
NR_052013.2:n.2468-159G>T
XM_011510357.1:c.2295-159G>T XP_011508659.1:n.2295-159G>T
XM_011510358.1:c.2424-159G>T XP_011508660.1:n.2424-159G>T
XM_011510359.1:c.1785-159G>T XP_011508661.1:n.1785-159G>T
XM_011510360.1:c.225-159G>T XP_011508662.1:n.225-159G>T
XM_011510361.1:c.216-159G>T XP_011508663.1:n.216-159G>T
XM_011510357.2:c.2295-159G>T XP_011508659.1:n.2295-159G>T
XM_011510358.2:c.2424-159G>T XP_011508660.1:n.2424-159G>T
XM_011510360.2:c.225-159G>T XP_011508662.1:n.225-159G>T
XM_011510361.2:c.216-159G>T XP_011508663.1:n.216-159G>T
XM_017004317.1:c.2424-159G>T XP_016859806.1:n.2424-159G>T
XM_024452961.1:c.1785-159G>T XP_024308729.1:n.1785-159G>T
NM_015909.4:c.2424-159G>T MANE Select NP_056993.2:n.2424-159G>T
NR_052013.3:n.2454-159G>T