Canonical Allele Identifier: CA355590406

Gene: DYNLT2B TM4SF19-DYNLT2B

Linked Data

• MyVariant Identifiers: chr3:g.196044933G>C (hg19) ; chr3:g.196318062G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.196318062G>C , CM000665.2:g.196318062G>C	GRCh38
NC_000003.11:g.196044933G>C , CM000665.1:g.196044933G>C	GRCh37
NC_000003.10:g.197529330G>C	NCBI36
NG_054930.1:g.5233C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325318.10:c.91C>G (DYNLT2B) MANE Select	ENSP00000324323.5:p.Leu31Val
ENST00000325318.9:c.91C>G (DYNLT2B)	ENSP00000324323.5:p.Leu31Val
ENST00000426563.5:c.91C>G (DYNLT2B)	ENSP00000415835.1:p.Leu31Val
ENST00000431391.1:c.91C>G	ENSP00000405181.1:p.Leu31Val
ENST00000442633.1:c.*74-1831C>G (TM4SF19-DYNLT2B)	ENSP00000405973.1:n.*74-1831C>G
ENST00000446494.1:c.91C>G (DYNLT2B)	ENSP00000410605.1:p.Leu31Val
NM_152773.4:c.91C>G (DYNLT2B)	NP_689986.2:p.Leu31Val
NR_037950.1:n.862-1831C>G (TM4SF19-DYNLT2B)
NM_001351628.1:c.91C>G (DYNLT2B)	NP_001338557.1:p.Leu31Val
NM_152773.5:c.91C>G (DYNLT2B) MANE Select	NP_689986.2:p.Leu31Val
NM_001351628.2:c.91C>G (DYNLT2B)	NP_001338557.1:p.Leu31Val