Canonical Allele Identifier: CA1176673423
Gene: SLC44A5 HGNC NCBI

Linked Data

dbSNP Id: rs1676402777

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75641006A>T , CM000663.2:g.75641006A>T GRCh38
NC_000001.10:g.76106691A>T , CM000663.1:g.76106691A>T GRCh37
NC_000001.9:g.75879279A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011540981.1:c.-74+68019T>A XP_011539283.1:n.-74+68019T>A
XM_011540982.1:c.-74+1367T>A XP_011539284.1:n.-74+1367T>A
XM_011540984.1:c.-70+1367T>A XP_011539286.1:n.-70+1367T>A
XM_017000609.1:c.-70+1367T>A XP_016856098.1:n.-70+1367T>A
XM_017000610.1:c.-70+1367T>A XP_016856099.1:n.-70+1367T>A