Canonical Allele Identifier: CA345884080
Gene: NBAS HGNC NCBI

Linked Data

dbSNP Id: rs1666777385
gnomAD v4: 2-15218832-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15218832T>G , CM000664.2:g.15218832T>G GRCh38
NC_000002.11:g.15358956T>G , CM000664.1:g.15358956T>G GRCh37
NC_000002.10:g.15276407T>G NCBI36
NG_032964.1:g.347517A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.4359A>C
ENST00000700062.1:c.4426+13590A>C
ENST00000700063.1:c.884A>C
ENST00000700064.1:c.2229A>C
ENST00000281513.10:c.6373A>C MANE Select ENSP00000281513.5:p.Lys2125Gln
ENST00000281513.9:c.6373A>C ENSP00000281513.5:p.Lys2125Gln
ENST00000417461.5:c.512+13590A>C ENSP00000392421.1:n.512+13590A>C
ENST00000442506.5:c.3516A>C
NM_015909.3:c.6373A>C NP_056993.2:p.Lys2125Gln
NR_052013.2:n.6280+13590A>C
XM_011510357.1:c.6244A>C XP_011508659.1:p.Lys2082Gln
XM_011510358.1:c.6373A>C XP_011508660.1:p.Lys2125Gln
XM_011510359.1:c.5734A>C XP_011508661.1:p.Lys1912Gln
XM_011510360.1:c.4174A>C XP_011508662.1:p.Lys1392Gln
XM_011510361.1:c.4165A>C XP_011508663.1:p.Lys1389Gln
XM_011510357.2:c.6244A>C XP_011508659.1:p.Lys2082Gln
XM_011510358.2:c.6373A>C XP_011508660.1:p.Lys2125Gln
XM_011510360.2:c.4174A>C XP_011508662.1:p.Lys1392Gln
XM_011510361.2:c.4165A>C XP_011508663.1:p.Lys1389Gln
XM_017004317.1:c.6373A>C XP_016859806.1:p.Lys2125Gln
XM_024452961.1:c.5734A>C XP_024308729.1:p.Lys1912Gln
NM_015909.4:c.6373A>C MANE Select NP_056993.2:p.Lys2125Gln
NR_052013.3:n.6266+13590A>C