Canonical Allele Identifier: CA904868812

Gene: DYNLT2B TM4SF19-DYNLT2B

Linked Data

• dbSNP Id: rs1351402665
• gnomAD v3: 3-196317953-T-C
• gnomAD v4: 3-196317953-T-C
• MyVariant Identifiers: chr3:g.196044824T>C (hg19) ; chr3:g.196317953T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.196317953T>C , CM000665.2:g.196317953T>C	GRCh38
NC_000003.11:g.196044824T>C , CM000665.1:g.196044824T>C	GRCh37
NC_000003.10:g.197529221T>C	NCBI36
NG_054930.1:g.5342A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325318.10:c.113+87A>G (DYNLT2B) MANE Select	ENSP00000324323.5:n.113+87A>G
ENST00000325318.9:c.113+87A>G (DYNLT2B)	ENSP00000324323.5:n.113+87A>G
ENST00000426563.5:c.117+83A>G (DYNLT2B)	ENSP00000415835.1:n.117+83A>G
ENST00000431391.1:c.113+87A>G	ENSP00000405181.1:n.113+87A>G
ENST00000442633.1:c.*74-1722A>G (TM4SF19-DYNLT2B)	ENSP00000405973.1:n.*74-1722A>G
ENST00000446494.1:c.113+87A>G (DYNLT2B)	ENSP00000410605.1:n.113+87A>G
NM_152773.4:c.113+87A>G (DYNLT2B)	NP_689986.2:n.113+87A>G
NR_037950.1:n.862-1722A>G (TM4SF19-DYNLT2B)
NM_001351628.1:c.113+87A>G (DYNLT2B)	NP_001338557.1:n.113+87A>G
XR_001740547.1:n.53A>G
NM_152773.5:c.113+87A>G (DYNLT2B) MANE Select	NP_689986.2:n.113+87A>G
NM_001351628.2:c.113+87A>G (DYNLT2B)	NP_001338557.1:n.113+87A>G