Canonical Allele Identifier: CA2261308338

Gene: SLC4A1

Linked Data

• dbSNP Id: rs539150676
• gnomAD v4: 17-44254747-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254747C>G , CM000679.2:g.44254747C>G	GRCh38
NC_000017.10:g.42332115C>G , CM000679.1:g.42332115C>G	GRCh37
NC_000017.9:g.39687641C>G	NCBI36
NG_007498.1:g.18388G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.1891-85G>C MANE Select	ENSP00000262418.6:n.1891-85G>C
ENST00000262418.10:c.1891-85G>C	ENSP00000262418.6:n.1891-85G>C
ENST00000399246.3:c.793-85G>C	ENSP00000382190.3:n.793-85G>C
NM_000342.3:c.1891-85G>C	NP_000333.1:n.1891-85G>C
XM_005257593.3:c.1696-85G>C	XP_005257650.1:n.1696-85G>C
XM_011525129.1:c.1801-85G>C	XP_011523431.1:n.1801-85G>C
XM_011525130.1:c.1891-85G>C	XP_011523432.1:n.1891-85G>C
XM_011525131.1:c.1891-85G>C	XP_011523433.1:n.1891-85G>C
XM_005257593.5:c.1696-85G>C	XP_005257650.1:n.1696-85G>C
XM_011525129.2:c.1801-85G>C	XP_011523431.1:n.1801-85G>C
NM_000342.4:c.1891-85G>C MANE Select	NP_000333.1:n.1891-85G>C