Canonical Allele Identifier: CA2696402280
Gene: SLC44A5 HGNC NCBI

Linked Data

dbSNP Id: rs2102221191

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75641079A>G , CM000663.2:g.75641079A>G GRCh38
NC_000001.10:g.76106764A>G , CM000663.1:g.76106764A>G GRCh37
NC_000001.9:g.75879352A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540981.1:c.-74+67946T>C XP_011539283.1:n.-74+67946T>C
XM_011540982.1:c.-74+1294T>C XP_011539284.1:n.-74+1294T>C
XM_011540984.1:c.-70+1294T>C XP_011539286.1:n.-70+1294T>C
XM_017000609.1:c.-70+1294T>C XP_016856098.1:n.-70+1294T>C
XM_017000610.1:c.-70+1294T>C XP_016856099.1:n.-70+1294T>C