Canonical Allele Identifier: CA2038688647

Gene: NAB2

Linked Data

• dbSNP Id: rs2033298580

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57094586_57094587del , CM000674.2:g.57094586_57094587del	GRCh38
NC_000012.11:g.57488369_57488370del , CM000674.1:g.57488369_57488370del	GRCh37
NC_000012.10:g.55774636_55774637del	NCBI36
NG_021272.1:g.21829_21830del
NG_021272.2:g.42555_42556del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300131.8:c.1469-26_1469-25del MANE Select	ENSP00000300131.3:n.1469-26_1469-25del
ENST00000300131.7:c.1469-26_1469-25del	ENSP00000300131.3:n.1469-26_1469-25del
ENST00000342556.6:c.1277-26_1277-25del	ENSP00000341491.6:n.1277-26_1277-25del
NM_005967.3:c.1469-26_1469-25del	NP_005958.1:n.1469-26_1469-25del
XM_005268894.2:c.1277-26_1277-25del	XP_005268951.1:n.1277-26_1277-25del
NM_001330305.1:c.1277-26_1277-25del	NP_001317234.1:n.1277-26_1277-25del
NM_005967.4:c.1469-26_1469-25del MANE Select	NP_005958.1:n.1469-26_1469-25del
NM_001330305.2:c.1277-26_1277-25del	NP_001317234.1:n.1277-26_1277-25del