Canonical Allele Identifier: CA772278622

Gene: SLC4A1

Linked Data

• dbSNP Id: rs1482742200
• gnomAD v3: 17-44254204-G-C
• gnomAD v4: 17-44254204-G-C
• MyVariant Identifiers: chr17:g.42331572G>C (hg19) ; chr17:g.44254204G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254204G>C , CM000679.2:g.44254204G>C	GRCh38
NC_000017.10:g.42331572G>C , CM000679.1:g.42331572G>C	GRCh37
NC_000017.9:g.39687098G>C	NCBI36
NG_007498.1:g.18931C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2057+292C>G MANE Select	ENSP00000262418.6:n.2057+292C>G
ENST00000262418.10:c.2057+292C>G	ENSP00000262418.6:n.2057+292C>G
ENST00000399246.3:c.959+292C>G	ENSP00000382190.3:n.959+292C>G
NM_000342.3:c.2057+292C>G	NP_000333.1:n.2057+292C>G
XM_005257593.3:c.1862+292C>G	XP_005257650.1:n.1862+292C>G
XM_011525129.1:c.1967+292C>G	XP_011523431.1:n.1967+292C>G
XM_011525130.1:c.2057+292C>G	XP_011523432.1:n.2057+292C>G
XM_011525131.1:c.2057+292C>G	XP_011523433.1:n.2057+292C>G
XM_005257593.5:c.1862+292C>G	XP_005257650.1:n.1862+292C>G
XM_011525129.2:c.1967+292C>G	XP_011523431.1:n.1967+292C>G
NM_000342.4:c.2057+292C>G MANE Select	NP_000333.1:n.2057+292C>G