Canonical Allele Identifier: CA1176673435
Gene: SLC44A5 HGNC NCBI

Linked Data

dbSNP Id: rs889063391

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75641024A>G , CM000663.2:g.75641024A>G GRCh38
NC_000001.10:g.76106709A>G , CM000663.1:g.76106709A>G GRCh37
NC_000001.9:g.75879297A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011540981.1:c.-74+68001T>C XP_011539283.1:n.-74+68001T>C
XM_011540982.1:c.-74+1349T>C XP_011539284.1:n.-74+1349T>C
XM_011540984.1:c.-70+1349T>C XP_011539286.1:n.-70+1349T>C
XM_017000609.1:c.-70+1349T>C XP_016856098.1:n.-70+1349T>C
XM_017000610.1:c.-70+1349T>C XP_016856099.1:n.-70+1349T>C