Canonical Allele Identifier: CA772273708
Gene: SLC4A1 HGNC NCBI

Linked Data

dbSNP Id: rs1351438248
gnomAD v3: 17-44249013-C-T
gnomAD v4: 17-44249013-C-T
MyVariant Identifiers: chr17:g.42326381C>T (hg19) chr17:g.44249013C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44249013C>T , CM000679.2:g.44249013C>T GRCh38
NC_000017.10:g.42326381C>T , CM000679.1:g.42326381C>T GRCh37
NC_000017.9:g.39681907C>T NCBI36
NG_007498.1:g.24122G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.*1445G>A MANE Select ENSP00000262418.6:n.*1445G>A
ENST00000262418.10:c.*1445G>A ENSP00000262418.6:n.*1445G>A
ENST00000399246.3:c.*1445G>A ENSP00000382190.3:n.*1445G>A
ENST00000631130.1:c.*81G>A ENSP00000486787.1:n.*81G>A
NM_000342.3:c.*1445G>A NP_000333.1:n.*1445G>A
XM_005257593.3:c.*1445G>A XP_005257650.1:n.*1445G>A
XM_011525129.1:c.*1445G>A XP_011523431.1:n.*1445G>A
NM_000342.4:c.*1445G>A MANE Select NP_000333.1:n.*1445G>A
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