Canonical Allele Identifier: CA345890208

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15564568T>G (hg19) ; chr2:g.15424444T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424444T>G , CM000664.2:g.15424444T>G	GRCh38
NC_000002.11:g.15564568T>G , CM000664.1:g.15564568T>G	GRCh37
NC_000002.10:g.15482019T>G	NCBI36
NG_032964.1:g.141905A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.545A>C
ENST00000700062.1:c.545A>C
ENST00000700065.1:n.2461A>C
ENST00000700066.1:c.1965A>C	ENSP00000514780.1:p.Gln655His
ENST00000281513.10:c.2448A>C MANE Select	ENSP00000281513.5:p.Gln816His
ENST00000281513.9:c.2448A>C	ENSP00000281513.5:p.Gln816His
NM_015909.3:c.2448A>C	NP_056993.2:p.Gln816His
NR_052013.2:n.2492A>C
XM_011510357.1:c.2319A>C	XP_011508659.1:p.Gln773His
XM_011510358.1:c.2448A>C	XP_011508660.1:p.Gln816His
XM_011510359.1:c.1809A>C	XP_011508661.1:p.Gln603His
XM_011510360.1:c.249A>C	XP_011508662.1:p.Gln83His
XM_011510361.1:c.240A>C	XP_011508663.1:p.Gln80His
XM_011510357.2:c.2319A>C	XP_011508659.1:p.Gln773His
XM_011510358.2:c.2448A>C	XP_011508660.1:p.Gln816His
XM_011510360.2:c.249A>C	XP_011508662.1:p.Gln83His
XM_011510361.2:c.240A>C	XP_011508663.1:p.Gln80His
XM_017004317.1:c.2448A>C	XP_016859806.1:p.Gln816His
XM_024452961.1:c.1809A>C	XP_024308729.1:p.Gln603His
NM_015909.4:c.2448A>C MANE Select	NP_056993.2:p.Gln816His
NR_052013.3:n.2478A>C