Canonical Allele Identifier: CA500288550
Gene: SLC4A1 HGNC NCBI

Linked Data

dbSNP Id: rs2144619982
MyVariant Identifiers: chr17:g.42337780A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44260412A>G , CM000679.2:g.44260412A>G GRCh38
NC_000017.10:g.42337780A>G , CM000679.1:g.42337780A>G GRCh37
NC_000017.9:g.39693306A>G NCBI36
NG_007498.1:g.12723T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262418.12:c.477T>C MANE Select ENSP00000262418.6:p.Leu159=
ENST00000262418.10:c.477T>C ENSP00000262418.6:p.Leu159=
ENST00000399246.3:c.477T>C ENSP00000382190.3:p.Leu159=
ENST00000471005.5:n.411T>C
ENST00000497360.5:n.616T>C
NM_000342.3:c.477T>C NP_000333.1:p.Leu159=
XM_005257593.3:c.282T>C XP_005257650.1:p.Leu94=
XM_011525129.1:c.477T>C XP_011523431.1:p.Leu159=
XM_011525130.1:c.477T>C XP_011523432.1:p.Leu159=
XM_011525131.1:c.477T>C XP_011523433.1:p.Leu159=
XM_005257593.5:c.282T>C XP_005257650.1:p.Leu94=
XM_011525129.2:c.477T>C XP_011523431.1:p.Leu159=
NM_000342.4:c.477T>C MANE Select NP_000333.1:p.Leu159=