Canonical Allele Identifier: CA345890206

Gene: NBAS

Linked Data

• dbSNP Id: rs1216893226
• gnomAD v2: 2-15564567-C-T
• gnomAD v3: 2-15424443-C-T
• gnomAD v4: 2-15424443-C-T
• MyVariant Identifiers: chr2:g.15564567C>T (hg19) ; chr2:g.15424443C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424443C>T , CM000664.2:g.15424443C>T	GRCh38
NC_000002.11:g.15564567C>T , CM000664.1:g.15564567C>T	GRCh37
NC_000002.10:g.15482018C>T	NCBI36
NG_032964.1:g.141906G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.546G>A
ENST00000700062.1:c.546G>A
ENST00000700065.1:n.2462G>A
ENST00000700066.1:c.1966G>A	ENSP00000514780.1:p.Asp656Asn
ENST00000281513.10:c.2449G>A MANE Select	ENSP00000281513.5:p.Asp817Asn
ENST00000281513.9:c.2449G>A	ENSP00000281513.5:p.Asp817Asn
NM_015909.3:c.2449G>A	NP_056993.2:p.Asp817Asn
NR_052013.2:n.2493G>A
XM_011510357.1:c.2320G>A	XP_011508659.1:p.Asp774Asn
XM_011510358.1:c.2449G>A	XP_011508660.1:p.Asp817Asn
XM_011510359.1:c.1810G>A	XP_011508661.1:p.Asp604Asn
XM_011510360.1:c.250G>A	XP_011508662.1:p.Asp84Asn
XM_011510361.1:c.241G>A	XP_011508663.1:p.Asp81Asn
XM_011510357.2:c.2320G>A	XP_011508659.1:p.Asp774Asn
XM_011510358.2:c.2449G>A	XP_011508660.1:p.Asp817Asn
XM_011510360.2:c.250G>A	XP_011508662.1:p.Asp84Asn
XM_011510361.2:c.241G>A	XP_011508663.1:p.Asp81Asn
XM_017004317.1:c.2449G>A	XP_016859806.1:p.Asp817Asn
XM_024452961.1:c.1810G>A	XP_024308729.1:p.Asp604Asn
NM_015909.4:c.2449G>A MANE Select	NP_056993.2:p.Asp817Asn
NR_052013.3:n.2479G>A