Canonical Allele Identifier: CA759128927
Gene: NBAS HGNC NCBI

Linked Data

dbSNP Id: rs1406206560
gnomAD v3: 2-15424662-T-A
gnomAD v4: 2-15424662-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424662T>A , CM000664.2:g.15424662T>A GRCh38
NC_000002.11:g.15564786T>A , CM000664.1:g.15564786T>A GRCh37
NC_000002.10:g.15482237T>A NCBI36
NG_032964.1:g.141687A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.521-194A>T
ENST00000700062.1:c.521-194A>T
ENST00000700065.1:n.2437-194A>T
ENST00000700066.1:c.1941-194A>T ENSP00000514780.1:n.1941-194A>T
ENST00000281513.10:c.2424-194A>T MANE Select ENSP00000281513.5:n.2424-194A>T
ENST00000281513.9:c.2424-194A>T ENSP00000281513.5:n.2424-194A>T
NM_015909.3:c.2424-194A>T NP_056993.2:n.2424-194A>T
NR_052013.2:n.2468-194A>T
XM_011510357.1:c.2295-194A>T XP_011508659.1:n.2295-194A>T
XM_011510358.1:c.2424-194A>T XP_011508660.1:n.2424-194A>T
XM_011510359.1:c.1785-194A>T XP_011508661.1:n.1785-194A>T
XM_011510360.1:c.225-194A>T XP_011508662.1:n.225-194A>T
XM_011510361.1:c.216-194A>T XP_011508663.1:n.216-194A>T
XM_011510357.2:c.2295-194A>T XP_011508659.1:n.2295-194A>T
XM_011510358.2:c.2424-194A>T XP_011508660.1:n.2424-194A>T
XM_011510360.2:c.225-194A>T XP_011508662.1:n.225-194A>T
XM_011510361.2:c.216-194A>T XP_011508663.1:n.216-194A>T
XM_017004317.1:c.2424-194A>T XP_016859806.1:n.2424-194A>T
XM_024452961.1:c.1785-194A>T XP_024308729.1:n.1785-194A>T
NM_015909.4:c.2424-194A>T MANE Select NP_056993.2:n.2424-194A>T
NR_052013.3:n.2454-194A>T