Canonical Allele Identifier: CA396938709
Gene: SLC38A8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.84065535A>G (hg19) chr16:g.84031930A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031930A>G , CM000678.2:g.84031930A>G GRCh38
NC_000016.9:g.84065535A>G , CM000678.1:g.84065535A>G GRCh37
NC_000016.8:g.82623036A>G NCBI36
NG_034136.1:g.15228T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.569T>C MANE Select ENSP00000299709.3:p.Val190Ala
ENST00000299709.7:c.569T>C ENSP00000299709.3:p.Val190Ala
ENST00000568178.1:c.569T>C ENSP00000457737.1:p.Val190Ala
NM_001080442.2:c.569T>C NP_001073911.1:p.Val190Ala
XM_011522872.1:c.569T>C XP_011521174.1:p.Val190Ala
XM_017022946.1:c.569T>C XP_016878435.1:p.Val190Ala
NM_001080442.3:c.569T>C MANE Select NP_001073911.1:p.Val190Ala
Search 100 bp 5'
Search 100 bp 3'