Canonical Allele Identifier: CA223629213

Gene: SLC22A8

Linked Data

• dbSNP Id: rs931277847
• gnomAD v3: 11-63003739-T-G
• gnomAD v4: 11-63003739-T-G
• MyVariant Identifiers: chr11:g.62771211T>G (hg19) ; chr11:g.63003739T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.63003739T>G , CM000673.2:g.63003739T>G	GRCh38
NC_000011.9:g.62771211T>G , CM000673.1:g.62771211T>G	GRCh37
NC_000011.8:g.62527787T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.334-2916A>C MANE Select	ENSP00000337335.2:n.334-2916A>C
ENST00000311438.12:c.334-2916A>C	ENSP00000311463.8:n.334-2916A>C
ENST00000336232.6:c.334-2916A>C	ENSP00000337335.2:n.334-2916A>C
ENST00000430500.6:c.334-2916A>C	ENSP00000398548.2:n.334-2916A>C
ENST00000535878.5:c.-36-2916A>C	ENSP00000443368.1:n.-36-2916A>C
ENST00000545207.5:c.61-2916A>C	ENSP00000441658.1:n.61-2916A>C
NM_001184732.1:c.334-2916A>C	NP_001171661.1:n.334-2916A>C
NM_001184733.1:c.61-2916A>C	NP_001171662.1:n.61-2916A>C
NM_001184736.1:c.-36-2916A>C	NP_001171665.1:n.-36-2916A>C
NM_004254.3:c.334-2916A>C	NP_004245.2:n.334-2916A>C
NM_004254.4:c.334-2916A>C MANE Select	NP_004245.2:n.334-2916A>C
NM_001184732.2:c.334-2916A>C	NP_001171661.1:n.334-2916A>C
NM_001184733.2:c.61-2916A>C	NP_001171662.1:n.61-2916A>C
NM_001184736.2:c.-36-2916A>C	NP_001171665.1:n.-36-2916A>C