Canonical Allele Identifier: CA2038688737
Gene: NAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57094624G= , CM000674.2:g.57094624G= GRCh38
NC_000012.11:g.57488407G= , CM000674.1:g.57488407G= GRCh37
NC_000012.10:g.55774674G= NCBI36
NG_021272.1:g.21790C=
NG_021272.2:g.42516C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300131.8:c.1481G= MANE Select ENSP00000300131.3:p.Gly494=
ENST00000300131.7:c.1481G= ENSP00000300131.3:p.Gly494=
ENST00000342556.6:c.1289G= ENSP00000341491.6:p.Gly430=
NM_005967.3:c.1481G= NP_005958.1:p.Gly494=
XM_005268894.2:c.1289G= XP_005268951.1:p.Gly430=
NM_001330305.1:c.1289G= NP_001317234.1:p.Gly430=
NM_005967.4:c.1481G= MANE Select NP_005958.1:p.Gly494=
NM_001330305.2:c.1289G= NP_001317234.1:p.Gly430=