Canonical Allele Identifier: CA2736185874
Gene: SLC23A2 HGNC NCBI

Linked Data

dbSNP Id: rs2122247170

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4977122T>C , CM000682.2:g.4977122T>C GRCh38
NC_000020.10:g.4957768T>C , CM000682.1:g.4957768T>C GRCh37
NC_000020.9:g.4905768T>C NCBI36
NG_029959.1:g.29378A>G
NG_029959.2:g.38172A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338244.6:c.-281-6203A>G MANE Select ENSP00000344322.1:n.-281-6203A>G
ENST00000338244.5:c.-281-6203A>G ENSP00000344322.1:n.-281-6203A>G
ENST00000379333.5:c.-281-6203A>G ENSP00000368637.1:n.-281-6203A>G
ENST00000468355.5:n.90-6207A>G
NM_005116.5:c.-281-6203A>G NP_005107.4:n.-281-6203A>G
NM_203327.1:c.-281-6203A>G NP_976072.1:n.-281-6203A>G
XM_011529414.1:c.-277-6207A>G XP_011527716.1:n.-277-6207A>G
XM_011529417.1:c.-155+24284A>G XP_011527719.1:n.-155+24284A>G
NM_005116.6:c.-281-6203A>G MANE Select NP_005107.4:n.-281-6203A>G
NM_203327.2:c.-281-6203A>G NP_976072.1:n.-281-6203A>G