Canonical Allele Identifier: CA4570737
Gene: SLC4A2 HGNC NCBI

Linked Data

dbSNP Id: rs761089682

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151064296A>G , CM000669.2:g.151064296A>G GRCh38
NC_000007.13:g.150761383A>G , CM000669.1:g.150761383A>G GRCh37
NC_000007.12:g.150392316A>G NCBI36
NG_051947.1:g.11097A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000413384.7:c.146A>G MANE Select ENSP00000405600.2:p.Glu49Gly
ENST00000677246.1:c.146A>G ENSP00000504447.1:p.Glu49Gly
ENST00000310317.9:c.52-309A>G ENSP00000311402.5:n.52-309A>G
ENST00000392826.6:c.119A>G ENSP00000376571.2:p.Glu40Gly
ENST00000413384.6:c.146A>G ENSP00000405600.2:p.Glu49Gly
ENST00000461735.1:c.104A>G ENSP00000419164.1:p.Glu35Gly
ENST00000463414.5:c.146A>G ENSP00000418584.1:p.Glu49Gly
ENST00000482950.5:c.146A>G ENSP00000419379.1:p.Glu49Gly
ENST00000483786.5:c.146A>G ENSP00000417808.1:p.Glu49Gly
ENST00000485713.5:c.146A>G ENSP00000419412.1:p.Glu49Gly
ENST00000488420.1:c.146A>G ENSP00000417221.1:p.Glu49Gly
ENST00000490898.5:c.146A>G ENSP00000418114.1:p.Glu49Gly
ENST00000494125.1:n.381A>G
NM_001199692.1:c.146A>G NP_001186621.1:p.Glu49Gly
NM_001199693.1:c.119A>G NP_001186622.1:p.Glu40Gly
NM_001199694.1:c.104A>G NP_001186623.1:p.Glu35Gly
NM_003040.3:c.146A>G NP_003031.3:p.Glu49Gly
XM_006716094.2:c.146A>G XP_006716157.1:p.Glu49Gly
XM_011516497.1:c.146A>G XP_011514799.1:p.Glu49Gly
NM_001199692.2:c.146A>G NP_001186621.1:p.Glu49Gly
NM_001199694.2:c.104A>G NP_001186623.1:p.Glu35Gly
XM_006716094.3:c.146A>G XP_006716157.1:p.Glu49Gly
NM_003040.4:c.146A>G MANE Select NP_003031.3:p.Glu49Gly
NM_001199692.3:c.146A>G NP_001186621.1:p.Glu49Gly