Canonical Allele Identifier: CA803997686

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1341772881
• gnomAD v3: 5-132313553-G-C
• gnomAD v4: 5-132313553-G-C
• MyVariant Identifiers: chr5:g.131649246G>C (hg19) ; chr5:g.132313553G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313553G>C , CM000667.2:g.132313553G>C	GRCh38
NC_000005.9:g.131649246G>C , CM000667.1:g.131649246G>C	GRCh37
NC_000005.8:g.131677145G>C	NCBI36
NG_012129.1:g.24102G>C
NG_012129.2:g.24102G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.498-61G>C (SLC22A4) MANE Select	ENSP00000200652.3:n.498-61G>C
ENST00000200652.3:c.498-61G>C (SLC22A4)	ENSP00000200652.3:n.498-61G>C
ENST00000491257.1:n.302-61G>C (SLC22A4)
NM_003059.2:c.498-61G>C (SLC22A4)	NP_003050.2:n.498-61G>C
NR_110997.1:n.825-1300C>G (MIR3936HG)
XM_006714675.2:c.-31-61G>C (SLC22A4)	XP_006714738.1:n.-31-61G>C
XM_011543589.1:c.394-61G>C (SLC22A4)	XP_011541891.1:n.394-61G>C
XM_006714675.4:c.-31-61G>C (SLC22A4)	XP_006714738.1:n.-31-61G>C
XM_011543589.2:c.394-61G>C (SLC22A4)	XP_011541891.1:n.394-61G>C
XM_017009776.1:c.-31-61G>C (SLC22A4)	XP_016865265.1:n.-31-61G>C
NM_003059.3:c.498-61G>C (SLC22A4) MANE Select	NP_003050.2:n.498-61G>C