Canonical Allele Identifier: CA591081698

Gene: VAV2

Linked Data

• dbSNP Id: rs1158148087
• gnomAD v2: 9-136720751-C-T
• gnomAD v3: 9-133855629-C-T
• gnomAD v4: 9-133855629-C-T
• MyVariant Identifiers: chr9:g.136720751C>T (hg19) ; chr9:g.133855629C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133855629C>T , CM000671.2:g.133855629C>T	GRCh38
NC_000009.11:g.136720751C>T , CM000671.1:g.136720751C>T	GRCh37
NC_000009.10:g.135710572C>T	NCBI36
NG_029725.1:g.141696G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371850.8:c.380+5745G>A MANE Select	ENSP00000360916.3:n.380+5745G>A
ENST00000371850.7:c.380+5745G>A	ENSP00000360916.3:n.380+5745G>A
ENST00000371851.1:c.380+5745G>A	ENSP00000360917.1:n.380+5745G>A
ENST00000406606.7:c.380+5745G>A	ENSP00000385362.3:n.380+5745G>A
NM_001134398.1:c.380+5745G>A	NP_001127870.1:n.380+5745G>A
NM_003371.3:c.380+5745G>A	NP_003362.2:n.380+5745G>A
XM_005272213.1:c.380+5745G>A	XP_005272270.1:n.380+5745G>A
XM_006717277.1:c.380+5745G>A	XP_006717340.1:n.380+5745G>A
XM_011518983.1:c.380+5745G>A	XP_011517285.1:n.380+5745G>A
XM_011518984.1:c.380+5745G>A	XP_011517286.1:n.380+5745G>A
XM_017015108.1:c.380+5745G>A	XP_016870597.1:n.380+5745G>A
XM_017015109.1:c.380+5745G>A	XP_016870598.1:n.380+5745G>A
XM_017015110.1:c.380+5745G>A	XP_016870599.1:n.380+5745G>A
XM_017015111.1:c.380+5745G>A	XP_016870600.1:n.380+5745G>A
XM_017015112.1:c.380+5745G>A	XP_016870601.1:n.380+5745G>A
XM_017015113.1:c.380+5745G>A	XP_016870602.1:n.380+5745G>A
NM_001134398.2:c.380+5745G>A MANE Select	NP_001127870.1:n.380+5745G>A
NM_003371.4:c.380+5745G>A	NP_003362.2:n.380+5745G>A