Canonical Allele Identifier: CA127189170

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs913820565
• gnomAD v3: 5-132313467-A-G
• gnomAD v4: 5-132313467-A-G
• MyVariant Identifiers: chr5:g.131649160A>G (hg19) ; chr5:g.132313467A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313467A>G , CM000667.2:g.132313467A>G	GRCh38
NC_000005.9:g.131649160A>G , CM000667.1:g.131649160A>G	GRCh37
NC_000005.8:g.131677059A>G	NCBI36
NG_012129.1:g.24016A>G
NG_012129.2:g.24016A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.498-147A>G (SLC22A4) MANE Select	ENSP00000200652.3:n.498-147A>G
ENST00000200652.3:c.498-147A>G (SLC22A4)	ENSP00000200652.3:n.498-147A>G
ENST00000491257.1:n.302-147A>G (SLC22A4)
NM_003059.2:c.498-147A>G (SLC22A4)	NP_003050.2:n.498-147A>G
NR_110997.1:n.825-1214T>C (MIR3936HG)
XM_006714675.2:c.-31-147A>G (SLC22A4)	XP_006714738.1:n.-31-147A>G
XM_011543589.1:c.394-147A>G (SLC22A4)	XP_011541891.1:n.394-147A>G
XM_006714675.4:c.-31-147A>G (SLC22A4)	XP_006714738.1:n.-31-147A>G
XM_011543589.2:c.394-147A>G (SLC22A4)	XP_011541891.1:n.394-147A>G
XM_017009776.1:c.-31-147A>G (SLC22A4)	XP_016865265.1:n.-31-147A>G
NM_003059.3:c.498-147A>G (SLC22A4) MANE Select	NP_003050.2:n.498-147A>G