Canonical Allele Identifier: CA437775724
Gene: DYNLT2B HGNC NCBI
TM4SF19-DYNLT2B HGNC NCBI

Linked Data

gnomAD v4: 3-196318066-A-G
MyVariant Identifiers: chr3:g.196044937A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196318066A>G , CM000665.2:g.196318066A>G GRCh38
NC_000003.11:g.196044937A>G , CM000665.1:g.196044937A>G GRCh37
NC_000003.10:g.197529334A>G NCBI36
NG_054930.1:g.5229T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325318.10:c.87T>C (DYNLT2B) MANE Select ENSP00000324323.5:p.Tyr29=
ENST00000325318.9:c.87T>C (DYNLT2B) ENSP00000324323.5:p.Tyr29=
ENST00000426563.5:c.87T>C (DYNLT2B) ENSP00000415835.1:p.Tyr29=
ENST00000431391.1:c.87T>C ENSP00000405181.1:p.Tyr29=
ENST00000442633.1:c.*74-1835T>C (TM4SF19-DYNLT2B) ENSP00000405973.1:n.*74-1835T>C
ENST00000446494.1:c.87T>C (DYNLT2B) ENSP00000410605.1:p.Tyr29=
NM_152773.4:c.87T>C (DYNLT2B) NP_689986.2:p.Tyr29=
NR_037950.1:n.862-1835T>C (TM4SF19-DYNLT2B)
NM_001351628.1:c.87T>C (DYNLT2B) NP_001338557.1:p.Tyr29=
NM_152773.5:c.87T>C (DYNLT2B) MANE Select NP_689986.2:p.Tyr29=
NM_001351628.2:c.87T>C (DYNLT2B) NP_001338557.1:p.Tyr29=
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Search 100 bp 3'