Canonical Allele Identifier: CA402205268
Gene: SLC39A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36114273T>C , CM000680.2:g.36114273T>C GRCh38
NC_000018.9:g.33694236T>C , CM000680.1:g.33694236T>C GRCh37
NC_000018.8:g.31948234T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269187.10:c.1667A>G MANE Select ENSP00000269187.4:p.His556Arg
ENST00000269187.9:c.1667A>G ENSP00000269187.4:p.His556Arg
ENST00000440549.6:c.842A>G ENSP00000401139.1:p.His281Arg
ENST00000586829.1:c.368A>G ENSP00000467724.1:p.His123Arg
ENST00000590986.5:c.1667A>G ENSP00000465915.1:p.His556Arg
NM_001099406.1:c.842A>G NP_001092876.1:p.His281Arg
NM_012319.3:c.1667A>G NP_036451.3:p.His556Arg
XM_011525900.1:c.1667A>G XP_011524202.1:p.His556Arg
XM_011525901.1:c.1667A>G XP_011524203.1:p.His556Arg
XM_011525900.2:c.1667A>G XP_011524202.1:p.His556Arg
XM_011525901.2:c.1667A>G XP_011524203.1:p.His556Arg
NM_012319.4:c.1667A>G MANE Select NP_036451.4:p.His556Arg
NM_001099406.2:c.842A>G NP_001092876.1:p.His281Arg