Canonical Allele Identifier: CA285457659
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs567497495
gnomAD v3: 16-84032211-C-T
gnomAD v4: 16-84032211-C-T
MyVariant Identifiers: chr16:g.84065816C>T (hg19) chr16:g.84032211C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84032211C>T , CM000678.2:g.84032211C>T GRCh38
NC_000016.9:g.84065816C>T , CM000678.1:g.84065816C>T GRCh37
NC_000016.8:g.82623317C>T NCBI36
NG_034136.1:g.14947G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.531-243G>A MANE Select ENSP00000299709.3:n.531-243G>A
ENST00000299709.7:c.531-243G>A ENSP00000299709.3:n.531-243G>A
ENST00000568178.1:c.531-243G>A ENSP00000457737.1:n.531-243G>A
NM_001080442.2:c.531-243G>A NP_001073911.1:n.531-243G>A
XM_011522872.1:c.531-243G>A XP_011521174.1:n.531-243G>A
XM_017022946.1:c.531-243G>A XP_016878435.1:n.531-243G>A
NM_001080442.3:c.531-243G>A MANE Select NP_001073911.1:n.531-243G>A
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