Canonical Allele Identifier: CA14514418
Gene: SLC39A6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36129254G>A , CM000680.2:g.36129254G>A GRCh38
NC_000018.9:g.33709217G>A , CM000680.1:g.33709217G>A GRCh37
NC_000018.8:g.31963215G>A NCBI36
NG_050745.1:g.4381G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269187.10:c.-150C>T MANE Select ENSP00000269187.4:n.-150C>T
ENST00000269187.9:c.-150C>T ENSP00000269187.4:n.-150C>T
ENST00000440549.6:c.-177C>T ENSP00000401139.1:n.-177C>T
ENST00000590986.5:c.-163C>T ENSP00000465915.1:n.-163C>T
NM_001099406.1:c.-177C>T NP_001092876.1:n.-177C>T
NM_012319.3:c.-150C>T NP_036451.3:n.-150C>T
XM_011525900.1:c.-163C>T XP_011524202.1:n.-163C>T
XM_011525901.1:c.-847C>T XP_011524203.1:n.-847C>T
XM_011525900.2:c.-163C>T XP_011524202.1:n.-163C>T
XM_011525901.2:c.-847C>T XP_011524203.1:n.-847C>T
NM_012319.4:c.-150C>T MANE Select NP_036451.4:n.-150C>T
NM_001099406.2:c.-177C>T NP_001092876.1:n.-177C>T
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