Canonical Allele Identifier: CA599649187

Gene: SLC22A12

Linked Data

• dbSNP Id: rs1223872622
• gnomAD v2: 11-64365979-C-T
• gnomAD v4: 11-64598507-C-T
• MyVariant Identifiers: chr11:g.64365979C>T (hg19) ; chr11:g.64598507C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598507C>T , CM000673.2:g.64598507C>T	GRCh38
NC_000011.9:g.64365979C>T , CM000673.1:g.64365979C>T	GRCh37
NC_000011.8:g.64122555C>T	NCBI36
NG_008110.1:g.12698C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.831-9C>T MANE Select	ENSP00000366797.1:n.831-9C>T
ENST00000336464.7:c.729-9C>T	ENSP00000336836.7:n.729-9C>T
ENST00000377567.6:c.507-9C>T	ENSP00000366790.2:n.507-9C>T
ENST00000377572.5:c.507-9C>T	ENSP00000366795.1:n.507-9C>T
ENST00000377574.5:c.831-9C>T	ENSP00000366797.1:n.831-9C>T
ENST00000473690.5:c.168-9C>T	ENSP00000438437.1:n.168-9C>T
NM_001276326.1:c.729-9C>T	NP_001263255.1:n.729-9C>T
NM_001276327.1:c.507-9C>T	NP_001263256.1:n.507-9C>T
NM_144585.3:c.831-9C>T	NP_653186.2:n.831-9C>T
NM_153378.2:c.168-9C>T	NP_700357.1:n.168-9C>T
XM_006718430.2:c.906-9C>T	XP_006718493.1:n.906-9C>T
XM_006718431.2:c.801-9C>T	XP_006718494.1:n.801-9C>T
XM_006718430.4:c.906-9C>T	XP_006718493.1:n.906-9C>T
XM_006718431.4:c.801-9C>T	XP_006718494.1:n.801-9C>T
NM_144585.4:c.831-9C>T MANE Select	NP_653186.2:n.831-9C>T
NM_001276326.2:c.729-9C>T	NP_001263255.1:n.729-9C>T
NM_153378.3:c.168-9C>T	NP_700357.1:n.168-9C>T
NM_001276327.2:c.507-9C>T	NP_001263256.1:n.507-9C>T