Canonical Allele Identifier: CA2730611339
Gene: PATL2 HGNC NCBI

Linked Data

dbSNP Id: rs1471185702

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711335G>A , CM000677.2:g.44711335G>A GRCh38
NC_000015.9:g.45003533G>A , CM000677.1:g.45003533G>A GRCh37
NC_000015.8:g.42790825G>A NCBI36
NG_012920.1:g.4849G>A
NG_012920.2:g.4859G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011521338.1:c.-569C>T XP_011519640.1:n.-569C>T
XM_011521339.1:c.-450C>T XP_011519641.1:n.-450C>T
XM_011521340.1:c.-391C>T XP_011519642.1:n.-391C>T
XM_011521343.1:c.-653C>T XP_011519645.1:n.-653C>T
XM_011521345.1:c.-624C>T XP_011519647.1:n.-624C>T
XM_011521338.3:c.-569C>T XP_011519640.1:n.-569C>T
XM_011521339.3:c.-450C>T XP_011519641.1:n.-450C>T
XM_011521340.3:c.-391C>T XP_011519642.1:n.-391C>T
XM_011521343.3:c.-653C>T XP_011519645.1:n.-653C>T
XM_011521345.3:c.-624C>T XP_011519647.1:n.-624C>T
NM_001387260.1:c.-79C>T NP_001374189.1:n.-79C>T