Canonical Allele Identifier: CA437775709

Gene: DYNLT2B TM4SF19-DYNLT2B

Linked Data

• gnomAD v4: 3-196318057-C-T
• MyVariant Identifiers: chr3:g.196044928C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.196318057C>T , CM000665.2:g.196318057C>T	GRCh38
NC_000003.11:g.196044928C>T , CM000665.1:g.196044928C>T	GRCh37
NC_000003.10:g.197529325C>T	NCBI36
NG_054930.1:g.5238G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325318.10:c.96G>A (DYNLT2B) MANE Select	ENSP00000324323.5:p.Arg32=
ENST00000325318.9:c.96G>A (DYNLT2B)	ENSP00000324323.5:p.Arg32=
ENST00000426563.5:c.96G>A (DYNLT2B)	ENSP00000415835.1:p.Arg32=
ENST00000431391.1:c.96G>A	ENSP00000405181.1:p.Arg32=
ENST00000442633.1:c.*74-1826G>A (TM4SF19-DYNLT2B)	ENSP00000405973.1:n.*74-1826G>A
ENST00000446494.1:c.96G>A (DYNLT2B)	ENSP00000410605.1:p.Arg32=
NM_152773.4:c.96G>A (DYNLT2B)	NP_689986.2:p.Arg32=
NR_037950.1:n.862-1826G>A (TM4SF19-DYNLT2B)
NM_001351628.1:c.96G>A (DYNLT2B)	NP_001338557.1:p.Arg32=
NM_152773.5:c.96G>A (DYNLT2B) MANE Select	NP_689986.2:p.Arg32=
NM_001351628.2:c.96G>A (DYNLT2B)	NP_001338557.1:p.Arg32=