Canonical Allele Identifier: CA1669341862
Gene: PHACTR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143640449G= , CM000668.2:g.143640449G= GRCh38
NC_000006.11:g.143961586G= , CM000668.1:g.143961586G= GRCh37
NC_000006.10:g.144003279G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305766.10:c.13+32127G= ENSP00000305530.6:n.13+32127G=
ENST00000367584.8:c.218-71567G= ENSP00000356556.4:n.218-71567G=
ENST00000427704.6:c.13+32127G= ENSP00000391763.2:n.13+32127G=
NM_001100166.1:c.13+32127G= NP_001093636.1:n.13+32127G=
NM_014721.2:c.13+32127G= NP_055536.2:n.13+32127G=
NM_001100166.2:c.13+32127G= NP_001093636.1:n.13+32127G=
NM_014721.3:c.13+32127G= NP_055536.2:n.13+32127G=
NM_001394736.1:c.218-71567G= NP_001381665.1:n.218-71567G=
NM_001394738.1:c.13+32127G= NP_001381667.1:n.13+32127G=
NR_172204.1:n.143+32127G=
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