Canonical Allele Identifier: CA2300269878
Gene: SLC14A2 HGNC NCBI

Linked Data

dbSNP Id: rs1599583240
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Genomic Alleles

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

Transcript Alleles

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