Canonical Allele Identifier: CA1259786402
Community Standard Title: NM_012476.3(VAX2):c.247+5016G=
Gene: VAX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70905884G= , CM000664.2:g.70905884G= GRCh38
NC_000002.11:g.71133014G= , CM000664.1:g.71133014G= GRCh37
NC_000002.10:g.70986522G= NCBI36
NG_030009.1:g.10295G=

Transcript Alleles

HGVS Amino-acid Change
NM_012476.3:c.247+5016G= MANE Select NP_036608.1:n.247+5016G=
ENST00000234392.3:c.247+5016G= MANE Select ENSP00000234392.2:n.247+5016G=
NM_012476.2:c.247+5016G= NP_036608.1:n.247+5016G=
ENST00000234392.2:c.247+5016G= ENSP00000234392.2:n.247+5016G=
ENST00000432367.6:c.71+5016G=
XM_006711982.2:c.247+5016G= XP_006712045.1:n.247+5016G=
XM_006711982.4:c.247+5016G= XP_006712045.1:n.247+5016G=
XM_011532749.1:c.247+5016G= XP_011531051.1:n.247+5016G=
XM_011532750.1:c.247+5016G= XP_011531052.1:n.247+5016G=
XM_011532750.3:c.247+5016G= XP_011531052.1:n.247+5016G=
XM_011532751.1:c.247+5016G= XP_011531053.1:n.247+5016G=
XM_011532751.3:c.247+5016G= XP_011531053.1:n.247+5016G=
XM_011532752.1:c.247+5016G= XP_011531054.1:n.247+5016G=