Canonical Allele Identifier: CA1669333787
Gene: PHACTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143622177T= , CM000668.2:g.143622177T= GRCh38
NC_000006.11:g.143943314T= , CM000668.1:g.143943314T= GRCh37
NC_000006.10:g.143985007T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305766.10:c.13+13855T= ENSP00000305530.6:n.13+13855T=
ENST00000367584.8:c.217+84970T= ENSP00000356556.4:n.217+84970T=
ENST00000427704.6:c.13+13855T= ENSP00000391763.2:n.13+13855T=
NM_001100166.1:c.13+13855T= NP_001093636.1:n.13+13855T=
NM_014721.2:c.13+13855T= NP_055536.2:n.13+13855T=
NM_001100166.2:c.13+13855T= NP_001093636.1:n.13+13855T=
NM_014721.3:c.13+13855T= NP_055536.2:n.13+13855T=
NM_001394736.1:c.217+84970T= NP_001381665.1:n.217+84970T=
NM_001394738.1:c.13+13855T= NP_001381667.1:n.13+13855T=
NR_172204.1:n.143+13855T=