Canonical Allele Identifier: CA2295937391
Gene: SLC39A6 HGNC NCBI

Linked Data

dbSNP Id: rs2089323219
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36114076A>T , CM000680.2:g.36114076A>T GRCh38
NC_000018.9:g.33694039A>T , CM000680.1:g.33694039A>T GRCh37
NC_000018.8:g.31948037A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000269187.10:c.1843+21T>A MANE Select ENSP00000269187.4:n.1843+21T>A
ENST00000269187.9:c.1843+21T>A ENSP00000269187.4:n.1843+21T>A
ENST00000440549.6:c.1018+21T>A ENSP00000401139.1:n.1018+21T>A
ENST00000586829.1:c.544+21T>A ENSP00000467724.1:n.544+21T>A
ENST00000590986.5:c.1843+21T>A ENSP00000465915.1:n.1843+21T>A
NM_001099406.1:c.1018+21T>A NP_001092876.1:n.1018+21T>A
NM_012319.3:c.1843+21T>A NP_036451.3:n.1843+21T>A
XM_011525900.1:c.1843+21T>A XP_011524202.1:n.1843+21T>A
XM_011525901.1:c.1843+21T>A XP_011524203.1:n.1843+21T>A
XM_011525900.2:c.1843+21T>A XP_011524202.1:n.1843+21T>A
XM_011525901.2:c.1843+21T>A XP_011524203.1:n.1843+21T>A
NM_012319.4:c.1843+21T>A MANE Select NP_036451.4:n.1843+21T>A
NM_001099406.2:c.1018+21T>A NP_001092876.1:n.1018+21T>A
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