Canonical Allele Identifier: CA725008230
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs554178168
MyVariant Identifiers: chr16:g.84065800T>G (hg19) chr16:g.84032195T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84032195T>G , CM000678.2:g.84032195T>G GRCh38
NC_000016.9:g.84065800T>G , CM000678.1:g.84065800T>G GRCh37
NC_000016.8:g.82623301T>G NCBI36
NG_034136.1:g.14963A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.531-227A>C MANE Select ENSP00000299709.3:n.531-227A>C
ENST00000299709.7:c.531-227A>C ENSP00000299709.3:n.531-227A>C
ENST00000568178.1:c.531-227A>C ENSP00000457737.1:n.531-227A>C
NM_001080442.2:c.531-227A>C NP_001073911.1:n.531-227A>C
XM_011522872.1:c.531-227A>C XP_011521174.1:n.531-227A>C
XM_017022946.1:c.531-227A>C XP_016878435.1:n.531-227A>C
NM_001080442.3:c.531-227A>C MANE Select NP_001073911.1:n.531-227A>C
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