Canonical Allele Identifier: CA2578789351
Gene: SLC22A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160249179C>A , CM000668.2:g.160249179C>A GRCh38
NC_000006.11:g.160670211C>A , CM000668.1:g.160670211C>A GRCh37
NC_000006.10:g.160590201C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366953.8:c.842+37G>T MANE Select ENSP00000355920.3:n.842+37G>T
ENST00000366952.1:c.779+37G>T ENSP00000355919.1:n.779+37G>T
ENST00000366953.7:c.842+37G>T ENSP00000355920.3:n.842+37G>T
ENST00000491092.1:n.739+37G>T
NM_003058.3:c.842+37G>T NP_003049.2:n.842+37G>T
NM_003058.4:c.842+37G>T MANE Select NP_003049.2:n.842+37G>T