Canonical Allele Identifier: CA437775712

Gene: DYNLT2B TM4SF19-DYNLT2B

Linked Data

• gnomAD v4: 3-196318059-G-T
• MyVariant Identifiers: chr3:g.196044930G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.196318059G>T , CM000665.2:g.196318059G>T	GRCh38
NC_000003.11:g.196044930G>T , CM000665.1:g.196044930G>T	GRCh37
NC_000003.10:g.197529327G>T	NCBI36
NG_054930.1:g.5236C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325318.10:c.94C>A (DYNLT2B) MANE Select	ENSP00000324323.5:p.Arg32=
ENST00000325318.9:c.94C>A (DYNLT2B)	ENSP00000324323.5:p.Arg32=
ENST00000426563.5:c.94C>A (DYNLT2B)	ENSP00000415835.1:p.Arg32=
ENST00000431391.1:c.94C>A	ENSP00000405181.1:p.Arg32=
ENST00000442633.1:c.*74-1828C>A (TM4SF19-DYNLT2B)	ENSP00000405973.1:n.*74-1828C>A
ENST00000446494.1:c.94C>A (DYNLT2B)	ENSP00000410605.1:p.Arg32=
NM_152773.4:c.94C>A (DYNLT2B)	NP_689986.2:p.Arg32=
NR_037950.1:n.862-1828C>A (TM4SF19-DYNLT2B)
NM_001351628.1:c.94C>A (DYNLT2B)	NP_001338557.1:p.Arg32=
NM_152773.5:c.94C>A (DYNLT2B) MANE Select	NP_689986.2:p.Arg32=
NM_001351628.2:c.94C>A (DYNLT2B)	NP_001338557.1:p.Arg32=