Canonical Allele Identifier: CA2038688265
Gene: NAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57094438C= , CM000674.2:g.57094438C= GRCh38
NC_000012.11:g.57488221C= , CM000674.1:g.57488221C= GRCh37
NC_000012.10:g.55774488C= NCBI36
NG_021272.1:g.21976G=
NG_021272.2:g.42702G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300131.8:c.1469-174C= MANE Select ENSP00000300131.3:n.1469-174C=
ENST00000300131.7:c.1469-174C= ENSP00000300131.3:n.1469-174C=
ENST00000342556.6:c.1277-174C= ENSP00000341491.6:n.1277-174C=
NM_005967.3:c.1469-174C= NP_005958.1:n.1469-174C=
XM_005268894.2:c.1277-174C= XP_005268951.1:n.1277-174C=
NM_001330305.1:c.1277-174C= NP_001317234.1:n.1277-174C=
NM_005967.4:c.1469-174C= MANE Select NP_005958.1:n.1469-174C=
NM_001330305.2:c.1277-174C= NP_001317234.1:n.1277-174C=