Canonical Allele Identifier: CA2300269877
Gene: SLC14A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45220242A= , CM000680.2:g.45220242A= GRCh38
NC_000018.9:g.42800207A= , CM000680.1:g.42800207A= GRCh37
NC_000018.8:g.41054205A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000586448.5:c.-125+7051A= ENSP00000465953.1:n.-125+7051A=
NM_001242692.1:c.-125+7051A= NP_001229621.1:n.-125+7051A=
XM_011526216.1:c.-251+7051A= XP_011524518.1:n.-251+7051A=
XM_017026016.2:c.-125+7051A= XP_016881505.1:n.-125+7051A=
XM_024451270.1:c.-125+7051A= XP_024307038.1:n.-125+7051A=
XM_024451271.1:c.-125+7051A= XP_024307039.1:n.-125+7051A=
NM_001242692.2:c.-125+7051A= NP_001229621.1:n.-125+7051A=
NM_001371319.1:c.-125+7051A= NP_001358248.1:n.-125+7051A=