Canonical Allele Identifier: CA42584245

Gene: NBAS

Linked Data

• dbSNP Id: rs980419373
• gnomAD v2: 2-15358873-A-G
• gnomAD v3: 2-15218749-A-G
• gnomAD v4: 2-15218749-A-G
• MyVariant Identifiers: chr2:g.15358873A>G (hg19) ; chr2:g.15218749A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218749A>G , CM000664.2:g.15218749A>G	GRCh38
NC_000002.11:g.15358873A>G , CM000664.1:g.15358873A>G	GRCh37
NC_000002.10:g.15276324A>G	NCBI36
NG_032964.1:g.347600T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4418+24T>C
ENST00000700062.1:c.4426+13673T>C
ENST00000700063.1:c.943+24T>C
ENST00000700064.1:c.2288+24T>C
ENST00000281513.10:c.6432+24T>C MANE Select	ENSP00000281513.5:n.6432+24T>C
ENST00000281513.9:c.6432+24T>C	ENSP00000281513.5:n.6432+24T>C
ENST00000417461.5:c.512+13673T>C	ENSP00000392421.1:n.512+13673T>C
ENST00000442506.5:c.3575+24T>C
NM_015909.3:c.6432+24T>C	NP_056993.2:n.6432+24T>C
NR_052013.2:n.6280+13673T>C
XM_011510357.1:c.6303+24T>C	XP_011508659.1:n.6303+24T>C
XM_011510358.1:c.6432+24T>C	XP_011508660.1:n.6432+24T>C
XM_011510359.1:c.5793+24T>C	XP_011508661.1:n.5793+24T>C
XM_011510360.1:c.4233+24T>C	XP_011508662.1:n.4233+24T>C
XM_011510361.1:c.4224+24T>C	XP_011508663.1:n.4224+24T>C
XM_011510357.2:c.6303+24T>C	XP_011508659.1:n.6303+24T>C
XM_011510358.2:c.6432+24T>C	XP_011508660.1:n.6432+24T>C
XM_011510360.2:c.4233+24T>C	XP_011508662.1:n.4233+24T>C
XM_011510361.2:c.4224+24T>C	XP_011508663.1:n.4224+24T>C
XM_017004317.1:c.6432+24T>C	XP_016859806.1:n.6432+24T>C
XM_024452961.1:c.5793+24T>C	XP_024308729.1:n.5793+24T>C
NM_015909.4:c.6432+24T>C MANE Select	NP_056993.2:n.6432+24T>C
NR_052013.3:n.6266+13673T>C