Canonical Allele Identifier: CA1027846697
Gene: NBAS HGNC NCBI

Linked Data

dbSNP Id: rs1677351197
gnomAD v3: 2-15424250-T-C
gnomAD v4: 2-15424250-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424250T>C , CM000664.2:g.15424250T>C GRCh38
NC_000002.11:g.15564374T>C , CM000664.1:g.15564374T>C GRCh37
NC_000002.10:g.15481825T>C NCBI36
NG_032964.1:g.142099A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.674+65A>G
ENST00000700062.1:c.674+65A>G
ENST00000700065.1:n.2590+65A>G
ENST00000700066.1:c.2094+65A>G ENSP00000514780.1:n.2094+65A>G
ENST00000281513.10:c.2577+65A>G MANE Select ENSP00000281513.5:n.2577+65A>G
ENST00000281513.9:c.2577+65A>G ENSP00000281513.5:n.2577+65A>G
ENST00000441755.5:c.78+65A>G ENSP00000396501.1:n.78+65A>G
ENST00000442506.5:c.80+65A>G
NM_015909.3:c.2577+65A>G NP_056993.2:n.2577+65A>G
NR_052013.2:n.2621+65A>G
XM_011510357.1:c.2448+65A>G XP_011508659.1:n.2448+65A>G
XM_011510358.1:c.2577+65A>G XP_011508660.1:n.2577+65A>G
XM_011510359.1:c.1938+65A>G XP_011508661.1:n.1938+65A>G
XM_011510360.1:c.378+65A>G XP_011508662.1:n.378+65A>G
XM_011510361.1:c.369+65A>G XP_011508663.1:n.369+65A>G
XM_011510357.2:c.2448+65A>G XP_011508659.1:n.2448+65A>G
XM_011510358.2:c.2577+65A>G XP_011508660.1:n.2577+65A>G
XM_011510360.2:c.378+65A>G XP_011508662.1:n.378+65A>G
XM_011510361.2:c.369+65A>G XP_011508663.1:n.369+65A>G
XM_017004317.1:c.2577+65A>G XP_016859806.1:n.2577+65A>G
XM_024452961.1:c.1938+65A>G XP_024308729.1:n.1938+65A>G
NM_015909.4:c.2577+65A>G MANE Select NP_056993.2:n.2577+65A>G
NR_052013.3:n.2607+65A>G