Canonical Allele Identifier: CA2734882823
Gene: SLC14A2 HGNC NCBI

Linked Data

dbSNP Id: rs2144342937

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45573928A>G , CM000680.2:g.45573928A>G GRCh38
NC_000018.9:g.43153893A>G , CM000680.1:g.43153893A>G GRCh37
NC_000018.8:g.41407891A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000586448.5:c.-34-50703A>G ENSP00000465953.1:n.-34-50703A>G
ENST00000589658.5:c.-34-50703A>G ENSP00000465349.2:n.-34-50703A>G
NM_001242692.1:c.-34-50703A>G NP_001229621.1:n.-34-50703A>G
XM_011526216.1:c.-160-15828A>G XP_011524518.1:n.-160-15828A>G
XM_011526217.1:c.-34-50703A>G XP_011524519.1:n.-34-50703A>G
XM_017026016.2:c.-34-50703A>G XP_016881505.1:n.-34-50703A>G
XM_024451270.1:c.-34-50703A>G XP_024307038.1:n.-34-50703A>G
XM_024451271.1:c.-34-50703A>G XP_024307039.1:n.-34-50703A>G
NM_001242692.2:c.-34-50703A>G NP_001229621.1:n.-34-50703A>G
NM_001371319.1:c.-34-50703A>G NP_001358248.1:n.-34-50703A>G