Canonical Allele Identifier: CA449704144
Gene: PPT2-EGFL8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32132357C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32164580C>G , CM000668.2:g.32164580C>G GRCh38
NC_000006.11:g.32132357C>G , CM000668.1:g.32132357C>G GRCh37
NC_000006.10:g.32240335C>G NCBI36
NG_042283.1:g.16129C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000421600.2:c.226C>G
ENST00000422437.5:c.767C>G ENSP00000457534.1:p.Pro256Arg
ENST00000428388.6:c.767C>G ENSP00000455087.1:p.Pro256Arg
ENST00000453656.6:n.898C>G
ENST00000479001.2:n.752C>G
ENST00000583227.5:c.*319C>G ENSP00000461909.1:n.*319C>G
ENST00000585246.5:c.*318-1558C>G ENSP00000463570.1:n.*318-1558C>G
NR_037861.1:n.1181C>G
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