Canonical Allele Identifier: CA2628214297
Gene: PATL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711325A>G , CM000677.2:g.44711325A>G GRCh38
NC_000015.9:g.45003523A>G , CM000677.1:g.45003523A>G GRCh37
NC_000015.8:g.42790815A>G NCBI36
NG_012920.1:g.4839A>G
NG_012920.2:g.4849A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011521338.1:c.-559T>C XP_011519640.1:n.-559T>C
XM_011521339.1:c.-440T>C XP_011519641.1:n.-440T>C
XM_011521340.1:c.-381T>C XP_011519642.1:n.-381T>C
XM_011521343.1:c.-643T>C XP_011519645.1:n.-643T>C
XM_011521345.1:c.-614T>C XP_011519647.1:n.-614T>C
XM_011521338.3:c.-559T>C XP_011519640.1:n.-559T>C
XM_011521339.3:c.-440T>C XP_011519641.1:n.-440T>C
XM_011521340.3:c.-381T>C XP_011519642.1:n.-381T>C
XM_011521343.3:c.-643T>C XP_011519645.1:n.-643T>C
XM_011521345.3:c.-614T>C XP_011519647.1:n.-614T>C
NM_001387260.1:c.-76+7T>C NP_001374189.1:n.-76+7T>C