Canonical Allele Identifier: CA503641293

Gene: SLC39A6

Linked Data

• MyVariant Identifiers: chr18:g.33694379C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114416C>T , CM000680.2:g.36114416C>T	GRCh38
NC_000018.9:g.33694379C>T , CM000680.1:g.33694379C>T	GRCh37
NC_000018.8:g.31948377C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1524G>A MANE Select	ENSP00000269187.4:p.Gln508=
ENST00000269187.9:c.1524G>A	ENSP00000269187.4:p.Gln508=
ENST00000440549.6:c.699G>A	ENSP00000401139.1:p.Gln233=
ENST00000586829.1:c.225G>A	ENSP00000467724.1:p.Gln75=
ENST00000590986.5:c.1524G>A	ENSP00000465915.1:p.Gln508=
NM_001099406.1:c.699G>A	NP_001092876.1:p.Gln233=
NM_012319.3:c.1524G>A	NP_036451.3:p.Gln508=
XM_011525900.1:c.1524G>A	XP_011524202.1:p.Gln508=
XM_011525901.1:c.1524G>A	XP_011524203.1:p.Gln508=
XM_011525900.2:c.1524G>A	XP_011524202.1:p.Gln508=
XM_011525901.2:c.1524G>A	XP_011524203.1:p.Gln508=
NM_012319.4:c.1524G>A MANE Select	NP_036451.4:p.Gln508=
NM_001099406.2:c.699G>A	NP_001092876.1:p.Gln233=