Canonical Allele Identifier: CA360812949
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1434516705

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340597A>T , CM000667.2:g.132340597A>T GRCh38
NC_000005.9:g.131676290A>T , CM000667.1:g.131676290A>T GRCh37
NC_000005.8:g.131704189A>T NCBI36
NG_012129.1:g.51146A>T
NG_012129.2:g.51146A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.1477A>T (SLC22A4) MANE Select ENSP00000200652.3:p.Met493Leu
ENST00000200652.3:c.1477A>T (SLC22A4) ENSP00000200652.3:p.Met493Leu
NM_003059.2:c.1477A>T (SLC22A4) NP_003050.2:p.Met493Leu
NR_110997.1:n.561-5671T>A (MIR3936HG)
XM_006714675.2:c.949A>T (SLC22A4) XP_006714738.1:p.Met317Leu
XM_011543589.1:c.1201A>T (SLC22A4) XP_011541891.1:p.Met401Leu
XM_006714675.4:c.949A>T (SLC22A4) XP_006714738.1:p.Met317Leu
XM_011543589.2:c.1201A>T (SLC22A4) XP_011541891.1:p.Met401Leu
XM_017009776.1:c.949A>T (SLC22A4) XP_016865265.1:p.Met317Leu
NM_003059.3:c.1477A>T (SLC22A4) MANE Select NP_003050.2:p.Met493Leu