Canonical Allele Identifier: CA355590373
Gene: DYNLT2B HGNC NCBI
TM4SF19-DYNLT2B HGNC NCBI

Linked Data

gnomAD v4: 3-196318056-G-T
MyVariant Identifiers: chr3:g.196044927G>T (hg19) chr3:g.196318056G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196318056G>T , CM000665.2:g.196318056G>T GRCh38
NC_000003.11:g.196044927G>T , CM000665.1:g.196044927G>T GRCh37
NC_000003.10:g.197529324G>T NCBI36
NG_054930.1:g.5239C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325318.10:c.97C>A (DYNLT2B) MANE Select ENSP00000324323.5:p.Pro33Thr
ENST00000325318.9:c.97C>A (DYNLT2B) ENSP00000324323.5:p.Pro33Thr
ENST00000426563.5:c.97C>A (DYNLT2B) ENSP00000415835.1:p.Pro33Thr
ENST00000431391.1:c.97C>A ENSP00000405181.1:p.Pro33Thr
ENST00000442633.1:c.*74-1825C>A (TM4SF19-DYNLT2B) ENSP00000405973.1:n.*74-1825C>A
ENST00000446494.1:c.97C>A (DYNLT2B) ENSP00000410605.1:p.Pro33Thr
NM_152773.4:c.97C>A (DYNLT2B) NP_689986.2:p.Pro33Thr
NR_037950.1:n.862-1825C>A (TM4SF19-DYNLT2B)
NM_001351628.1:c.97C>A (DYNLT2B) NP_001338557.1:p.Pro33Thr
NM_152773.5:c.97C>A (DYNLT2B) MANE Select NP_689986.2:p.Pro33Thr
NM_001351628.2:c.97C>A (DYNLT2B) NP_001338557.1:p.Pro33Thr
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