Canonical Allele Identifier: CA1583118307

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1750246536

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313614del , CM000667.2:g.132313614del	GRCh38
NC_000005.9:g.131649307del , CM000667.1:g.131649307del	GRCh37
NC_000005.8:g.131677206del	NCBI36
NG_012129.1:g.24163del
NG_012129.2:g.24163del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.498del (SLC22A4)
ENST00000200652.3:c.498del (SLC22A4)
ENST00000491257.1:n.302del (SLC22A4)
NM_003059.2:c.498del (SLC22A4)
NR_110997.1:n.825-1360del (MIR3936HG)
XM_006714675.2:c.-31del (SLC22A4)
XM_011543589.1:c.394del (SLC22A4)
XM_006714675.4:c.-31del (SLC22A4)
XM_011543589.2:c.394del (SLC22A4)
XM_017009776.1:c.-31del (SLC22A4)
NM_003059.3:c.498del (SLC22A4)