Canonical Allele Identifier: CA355590385
Gene: DYNLT2B HGNC NCBI
TM4SF19-DYNLT2B HGNC NCBI

Linked Data

gnomAD v4: 3-196318058-C-T
MyVariant Identifiers: chr3:g.196044929C>T (hg19) chr3:g.196318058C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196318058C>T , CM000665.2:g.196318058C>T GRCh38
NC_000003.11:g.196044929C>T , CM000665.1:g.196044929C>T GRCh37
NC_000003.10:g.197529326C>T NCBI36
NG_054930.1:g.5237G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325318.10:c.95G>A (DYNLT2B) MANE Select ENSP00000324323.5:p.Arg32Gln
ENST00000325318.9:c.95G>A (DYNLT2B) ENSP00000324323.5:p.Arg32Gln
ENST00000426563.5:c.95G>A (DYNLT2B) ENSP00000415835.1:p.Arg32Gln
ENST00000431391.1:c.95G>A ENSP00000405181.1:p.Arg32Gln
ENST00000442633.1:c.*74-1827G>A (TM4SF19-DYNLT2B) ENSP00000405973.1:n.*74-1827G>A
ENST00000446494.1:c.95G>A (DYNLT2B) ENSP00000410605.1:p.Arg32Gln
NM_152773.4:c.95G>A (DYNLT2B) NP_689986.2:p.Arg32Gln
NR_037950.1:n.862-1827G>A (TM4SF19-DYNLT2B)
NM_001351628.1:c.95G>A (DYNLT2B) NP_001338557.1:p.Arg32Gln
NM_152773.5:c.95G>A (DYNLT2B) MANE Select NP_689986.2:p.Arg32Gln
NM_001351628.2:c.95G>A (DYNLT2B) NP_001338557.1:p.Arg32Gln
Search 100 bp 5'
Search 100 bp 3'