Canonical Allele Identifier: CA629190677

Gene: SLC39A6

Linked Data

• dbSNP Id: rs1463785882
• gnomAD v2: 18-33694055-T-C
• gnomAD v4: 18-36114092-T-C
• MyVariant Identifiers: chr18:g.33694055T>C (hg19) ; chr18:g.36114092T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114092T>C , CM000680.2:g.36114092T>C	GRCh38
NC_000018.9:g.33694055T>C , CM000680.1:g.33694055T>C	GRCh37
NC_000018.8:g.31948053T>C	NCBI36

Transcript Alleles

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