Canonical Allele Identifier: CA2736185869
Gene: SLC23A2 HGNC NCBI

Linked Data

dbSNP Id: rs2122247012
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4977070A>G , CM000682.2:g.4977070A>G GRCh38
NC_000020.10:g.4957716A>G , CM000682.1:g.4957716A>G GRCh37
NC_000020.9:g.4905716A>G NCBI36
NG_029959.1:g.29430T>C
NG_029959.2:g.38224T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338244.6:c.-281-6151T>C MANE Select ENSP00000344322.1:n.-281-6151T>C
ENST00000338244.5:c.-281-6151T>C ENSP00000344322.1:n.-281-6151T>C
ENST00000379333.5:c.-281-6151T>C ENSP00000368637.1:n.-281-6151T>C
ENST00000468355.5:n.90-6155T>C
NM_005116.5:c.-281-6151T>C NP_005107.4:n.-281-6151T>C
NM_203327.1:c.-281-6151T>C NP_976072.1:n.-281-6151T>C
XM_011529414.1:c.-277-6155T>C XP_011527716.1:n.-277-6155T>C
XM_011529417.1:c.-155+24336T>C XP_011527719.1:n.-155+24336T>C
NM_005116.6:c.-281-6151T>C MANE Select NP_005107.4:n.-281-6151T>C
NM_203327.2:c.-281-6151T>C NP_976072.1:n.-281-6151T>C
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