Canonical Allele Identifier: CA820127644
Gene: PHACTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1207128591
MyVariant Identifiers: chr6:g.143961605G>A (hg19) chr6:g.143640468G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143640468G>A , CM000668.2:g.143640468G>A GRCh38
NC_000006.11:g.143961605G>A , CM000668.1:g.143961605G>A GRCh37
NC_000006.10:g.144003298G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305766.10:c.13+32146G>A ENSP00000305530.6:n.13+32146G>A
ENST00000367584.8:c.218-71548G>A ENSP00000356556.4:n.218-71548G>A
ENST00000427704.6:c.13+32146G>A ENSP00000391763.2:n.13+32146G>A
NM_001100166.1:c.13+32146G>A NP_001093636.1:n.13+32146G>A
NM_014721.2:c.13+32146G>A NP_055536.2:n.13+32146G>A
NM_001100166.2:c.13+32146G>A NP_001093636.1:n.13+32146G>A
NM_014721.3:c.13+32146G>A NP_055536.2:n.13+32146G>A
NM_001394736.1:c.218-71548G>A NP_001381665.1:n.218-71548G>A
NM_001394738.1:c.13+32146G>A NP_001381667.1:n.13+32146G>A
NR_172204.1:n.143+32146G>A
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