Canonical Allele Identifier: CA1669341854
Gene: PHACTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143640441T= , CM000668.2:g.143640441T= GRCh38
NC_000006.11:g.143961578T= , CM000668.1:g.143961578T= GRCh37
NC_000006.10:g.144003271T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305766.10:c.13+32119T= ENSP00000305530.6:n.13+32119T=
ENST00000367584.8:c.218-71575T= ENSP00000356556.4:n.218-71575T=
ENST00000427704.6:c.13+32119T= ENSP00000391763.2:n.13+32119T=
NM_001100166.1:c.13+32119T= NP_001093636.1:n.13+32119T=
NM_014721.2:c.13+32119T= NP_055536.2:n.13+32119T=
NM_001100166.2:c.13+32119T= NP_001093636.1:n.13+32119T=
NM_014721.3:c.13+32119T= NP_055536.2:n.13+32119T=
NM_001394736.1:c.218-71575T= NP_001381665.1:n.218-71575T=
NM_001394738.1:c.13+32119T= NP_001381667.1:n.13+32119T=
NR_172204.1:n.143+32119T=