Canonical Allele Identifier: CA446328919

Gene: SLC22A4 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131649445G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313752G>C , CM000667.2:g.132313752G>C	GRCh38
NC_000005.9:g.131649445G>C , CM000667.1:g.131649445G>C	GRCh37
NC_000005.8:g.131677344G>C	NCBI36
NG_012129.1:g.24301G>C
NG_012129.2:g.24301G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.636G>C (SLC22A4) MANE Select	ENSP00000200652.3:p.Val212=
ENST00000200652.3:c.636G>C (SLC22A4)	ENSP00000200652.3:p.Val212=
ENST00000491257.1:n.440G>C (SLC22A4)
NM_003059.2:c.636G>C (SLC22A4)	NP_003050.2:p.Val212=
NR_110997.1:n.825-1499C>G (MIR3936HG)
XM_006714675.2:c.108G>C (SLC22A4)	XP_006714738.1:p.Val36=
XM_011543589.1:c.532G>C (SLC22A4)	XP_011541891.1:p.Gly178Arg
XM_006714675.4:c.108G>C (SLC22A4)	XP_006714738.1:p.Val36=
XM_011543589.2:c.532G>C (SLC22A4)	XP_011541891.1:p.Gly178Arg
XM_017009776.1:c.108G>C (SLC22A4)	XP_016865265.1:p.Val36=
NM_003059.3:c.636G>C (SLC22A4) MANE Select	NP_003050.2:p.Val212=