Canonical Allele Identifier: CA496764402
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs1597271546
MyVariant Identifiers: chr16:g.84065477T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031872T>C , CM000678.2:g.84031872T>C GRCh38
NC_000016.9:g.84065477T>C , CM000678.1:g.84065477T>C GRCh37
NC_000016.8:g.82622978T>C NCBI36
NG_034136.1:g.15286A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.627A>G MANE Select ENSP00000299709.3:p.Ser209=
ENST00000299709.7:c.627A>G ENSP00000299709.3:p.Ser209=
ENST00000568178.1:c.627A>G ENSP00000457737.1:p.Ser209=
NM_001080442.2:c.627A>G NP_001073911.1:p.Ser209=
XM_011522872.1:c.627A>G XP_011521174.1:p.Ser209=
XM_017022946.1:c.627A>G XP_016878435.1:p.Ser209=
NM_001080442.3:c.627A>G MANE Select NP_001073911.1:p.Ser209=
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