Canonical Allele Identifier: CA360804068
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.131649424G>C (hg19) chr5:g.132313731G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132313731G>C , CM000667.2:g.132313731G>C GRCh38
NC_000005.9:g.131649424G>C , CM000667.1:g.131649424G>C GRCh37
NC_000005.8:g.131677323G>C NCBI36
NG_012129.1:g.24280G>C
NG_012129.2:g.24280G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.615G>C (SLC22A4) MANE Select ENSP00000200652.3:p.Met205Ile
ENST00000200652.3:c.615G>C (SLC22A4) ENSP00000200652.3:p.Met205Ile
ENST00000491257.1:n.419G>C (SLC22A4)
NM_003059.2:c.615G>C (SLC22A4) NP_003050.2:p.Met205Ile
NR_110997.1:n.825-1478C>G (MIR3936HG)
XM_006714675.2:c.87G>C (SLC22A4) XP_006714738.1:p.Met29Ile
XM_011543589.1:c.511G>C (SLC22A4) XP_011541891.1:p.Gly171Arg
XM_006714675.4:c.87G>C (SLC22A4) XP_006714738.1:p.Met29Ile
XM_011543589.2:c.511G>C (SLC22A4) XP_011541891.1:p.Gly171Arg
XM_017009776.1:c.87G>C (SLC22A4) XP_016865265.1:p.Met29Ile
NM_003059.3:c.615G>C (SLC22A4) MANE Select NP_003050.2:p.Met205Ile
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