Canonical Allele Identifier: CA3403707
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs753255483

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340613T>C , CM000667.2:g.132340613T>C GRCh38
NC_000005.9:g.131676306T>C , CM000667.1:g.131676306T>C GRCh37
NC_000005.8:g.131704205T>C NCBI36
NG_012129.1:g.51162T>C
NG_012129.2:g.51162T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.1493T>C (SLC22A4) MANE Select ENSP00000200652.3:p.Val498Ala
ENST00000200652.3:c.1493T>C (SLC22A4) ENSP00000200652.3:p.Val498Ala
NM_003059.2:c.1493T>C (SLC22A4) NP_003050.2:p.Val498Ala
NR_110997.1:n.561-5687A>G (MIR3936HG)
XM_006714675.2:c.965T>C (SLC22A4) XP_006714738.1:p.Val322Ala
XM_011543589.1:c.1217T>C (SLC22A4) XP_011541891.1:p.Val406Ala
XM_006714675.4:c.965T>C (SLC22A4) XP_006714738.1:p.Val322Ala
XM_011543589.2:c.1217T>C (SLC22A4) XP_011541891.1:p.Val406Ala
XM_017009776.1:c.965T>C (SLC22A4) XP_016865265.1:p.Val322Ala
NM_003059.3:c.1493T>C (SLC22A4) MANE Select NP_003050.2:p.Val498Ala