Canonical Allele Identifier: CA24590735
Gene: SLC44A5 HGNC NCBI

Linked Data

dbSNP Id: rs1030795410
gnomAD v3: 1-75641000-T-C
gnomAD v4: 1-75641000-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75641000T>C , CM000663.2:g.75641000T>C GRCh38
NC_000001.10:g.76106685T>C , CM000663.1:g.76106685T>C GRCh37
NC_000001.9:g.75879273T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011540981.1:c.-74+68025A>G XP_011539283.1:n.-74+68025A>G
XM_011540982.1:c.-74+1373A>G XP_011539284.1:n.-74+1373A>G
XM_011540984.1:c.-70+1373A>G XP_011539286.1:n.-70+1373A>G
XM_017000609.1:c.-70+1373A>G XP_016856098.1:n.-70+1373A>G
XM_017000610.1:c.-70+1373A>G XP_016856099.1:n.-70+1373A>G