Canonical Allele Identifier: CA984003163
Gene: SLC4A1 HGNC NCBI

Linked Data

dbSNP Id: rs763961316

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44249705G>C , CM000679.2:g.44249705G>C GRCh38
NC_000017.10:g.42327073G>C , CM000679.1:g.42327073G>C GRCh37
NC_000017.9:g.39682599G>C NCBI36
NG_007498.1:g.23430C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.*753C>G MANE Select ENSP00000262418.6:n.*753C>G
ENST00000262418.10:c.*753C>G ENSP00000262418.6:n.*753C>G
ENST00000399246.3:c.*753C>G ENSP00000382190.3:n.*753C>G
ENST00000631130.1:c.-455C>G ENSP00000486787.1:n.-455C>G
NM_000342.3:c.*753C>G NP_000333.1:n.*753C>G
XM_005257593.3:c.*753C>G XP_005257650.1:n.*753C>G
XM_011525129.1:c.*753C>G XP_011523431.1:n.*753C>G
XM_005257593.5:c.*753C>G XP_005257650.1:n.*753C>G
XM_011525129.2:c.*753C>G XP_011523431.1:n.*753C>G
NM_000342.4:c.*753C>G MANE Select NP_000333.1:n.*753C>G