Canonical Allele Identifier: CA1669341859
Gene: PHACTR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143640445G= , CM000668.2:g.143640445G= GRCh38
NC_000006.11:g.143961582G= , CM000668.1:g.143961582G= GRCh37
NC_000006.10:g.144003275G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305766.10:c.13+32123G= ENSP00000305530.6:n.13+32123G=
ENST00000367584.8:c.218-71571G= ENSP00000356556.4:n.218-71571G=
ENST00000427704.6:c.13+32123G= ENSP00000391763.2:n.13+32123G=
NM_001100166.1:c.13+32123G= NP_001093636.1:n.13+32123G=
NM_014721.2:c.13+32123G= NP_055536.2:n.13+32123G=
NM_001100166.2:c.13+32123G= NP_001093636.1:n.13+32123G=
NM_014721.3:c.13+32123G= NP_055536.2:n.13+32123G=
NM_001394736.1:c.218-71571G= NP_001381665.1:n.218-71571G=
NM_001394738.1:c.13+32123G= NP_001381667.1:n.13+32123G=
NR_172204.1:n.143+32123G=
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