Canonical Allele Identifier: CA384836521

Gene: DIP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50678807A>T , CM000674.2:g.50678807A>T	GRCh38
NC_000012.11:g.51072590A>T , CM000674.1:g.51072590A>T	GRCh37
NC_000012.10:g.49358857A>T	NCBI36
NG_021196.1:g.178823A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_173602.3:c.1045A>T MANE Select	NP_775873.2:p.Thr349Ser
ENST00000301180.10:c.1045A>T MANE Select	ENSP00000301180.5:p.Thr349Ser
NM_173602.2:c.1045A>T	NP_775873.2:p.Thr349Ser
ENST00000301180.9:c.1045A>T	ENSP00000301180.5:p.Thr349Ser
ENST00000546719.1:n.822A>T
ENST00000549620.5:n.1201A>T
XM_005269044.1:c.1048A>T	XP_005269101.1:p.Thr350Ser
XM_006719520.2:c.1075A>T	XP_006719583.1:p.Thr359Ser
XM_006719521.2:c.862A>T	XP_006719584.1:p.Thr288Ser
XM_006719522.2:c.694A>T	XP_006719585.1:p.Thr232Ser
XM_011538594.1:c.1078A>T	XP_011536896.1:p.Thr360Ser
XM_011538595.1:c.1078A>T	XP_011536897.1:p.Thr360Ser
XM_011538596.1:c.865A>T	XP_011536898.1:p.Thr289Ser