Canonical Allele Identifier: CA13102905
Gene: VAV2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133858398A>G , CM000671.2:g.133858398A>G GRCh38
NC_000009.11:g.136723520A>G , CM000671.1:g.136723520A>G GRCh37
NC_000009.10:g.135713341A>G NCBI36
NG_029725.1:g.138927T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371850.8:c.380+2976T>C MANE Select ENSP00000360916.3:n.380+2976T>C
ENST00000371850.7:c.380+2976T>C ENSP00000360916.3:n.380+2976T>C
ENST00000371851.1:c.380+2976T>C ENSP00000360917.1:n.380+2976T>C
ENST00000406606.7:c.380+2976T>C ENSP00000385362.3:n.380+2976T>C
NM_001134398.1:c.380+2976T>C NP_001127870.1:n.380+2976T>C
NM_003371.3:c.380+2976T>C NP_003362.2:n.380+2976T>C
XM_005272213.1:c.380+2976T>C XP_005272270.1:n.380+2976T>C
XM_006717277.1:c.380+2976T>C XP_006717340.1:n.380+2976T>C
XM_011518983.1:c.380+2976T>C XP_011517285.1:n.380+2976T>C
XM_011518984.1:c.380+2976T>C XP_011517286.1:n.380+2976T>C
XM_017015108.1:c.380+2976T>C XP_016870597.1:n.380+2976T>C
XM_017015109.1:c.380+2976T>C XP_016870598.1:n.380+2976T>C
XM_017015110.1:c.380+2976T>C XP_016870599.1:n.380+2976T>C
XM_017015111.1:c.380+2976T>C XP_016870600.1:n.380+2976T>C
XM_017015112.1:c.380+2976T>C XP_016870601.1:n.380+2976T>C
XM_017015113.1:c.380+2976T>C XP_016870602.1:n.380+2976T>C
NM_001134398.2:c.380+2976T>C MANE Select NP_001127870.1:n.380+2976T>C
NM_003371.4:c.380+2976T>C NP_003362.2:n.380+2976T>C
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