Canonical Allele Identifier: CA136901322
Gene: PPT2-EGFL8 HGNC NCBI

Linked Data

dbSNP Id: rs750500933
MyVariant Identifiers: chr6:g.32132024C>T (hg19) chr6:g.32164247C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32164247C>T , CM000668.2:g.32164247C>T GRCh38
NC_000006.11:g.32132024C>T , CM000668.1:g.32132024C>T GRCh37
NC_000006.10:g.32240002C>T NCBI36
NG_042283.1:g.15796C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000421600.2:c.225-332C>T
ENST00000422437.5:c.766-332C>T ENSP00000457534.1:n.766-332C>T
ENST00000428388.6:c.766-332C>T ENSP00000455087.1:n.766-332C>T
ENST00000453656.6:n.897-332C>T
ENST00000479001.2:n.751-332C>T
ENST00000583227.5:c.*318-332C>T ENSP00000461909.1:n.*318-332C>T
ENST00000585246.5:c.*317+1625C>T ENSP00000463570.1:n.*317+1625C>T
NR_037861.1:n.1180-332C>T
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