Canonical Allele Identifier: CA8939018
Gene: SLC39A6 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1050631

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36114157G>A , CM000680.2:g.36114157G>A GRCh38
NC_000018.9:g.33694120G>A , CM000680.1:g.33694120G>A GRCh37
NC_000018.8:g.31948118G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001099406.1:c.958C>T VV NP_001092876.1:p.Leu320=
NM_012319.3:c.1783C>T VV NP_036451.3:p.Leu595=
XM_011525900.1:c.1783C>T XP_011524202.1:p.Leu595=
XM_011525901.1:c.1783C>T XP_011524203.1:p.Leu595=
XM_011525900.2:c.1783C>T
XM_011525901.2:c.1783C>T
ENST00000269187.9:c.1783C>T ENSP00000269187.4:p.Leu595=
ENST00000440549.6:c.958C>T ENSP00000401139.1:p.Leu320=
ENST00000586829.1:c.484C>T ENSP00000467724.1:p.Leu162=
ENST00000590986.5:c.1783C>T ENSP00000465915.1:p.Leu595=