Canonical Allele Identifier: CA2038688226
Gene: NAB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57094429G= , CM000674.2:g.57094429G= GRCh38
NC_000012.11:g.57488212G= , CM000674.1:g.57488212G= GRCh37
NC_000012.10:g.55774479G= NCBI36
NG_021272.1:g.21985C=
NG_021272.2:g.42711C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300131.8:c.1469-183G= MANE Select ENSP00000300131.3:n.1469-183G=
ENST00000300131.7:c.1469-183G= ENSP00000300131.3:n.1469-183G=
ENST00000342556.6:c.1277-183G= ENSP00000341491.6:n.1277-183G=
NM_005967.3:c.1469-183G= NP_005958.1:n.1469-183G=
XM_005268894.2:c.1277-183G= XP_005268951.1:n.1277-183G=
NM_001330305.1:c.1277-183G= NP_001317234.1:n.1277-183G=
NM_005967.4:c.1469-183G= MANE Select NP_005958.1:n.1469-183G=
NM_001330305.2:c.1277-183G= NP_001317234.1:n.1277-183G=
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