Canonical Allele Identifier: CA396938617
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs2085244713

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031913A>G , CM000678.2:g.84031913A>G GRCh38
NC_000016.9:g.84065518A>G , CM000678.1:g.84065518A>G GRCh37
NC_000016.8:g.82623019A>G NCBI36
NG_034136.1:g.15245T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.586T>C MANE Select ENSP00000299709.3:p.Tyr196His
ENST00000299709.7:c.586T>C ENSP00000299709.3:p.Tyr196His
ENST00000568178.1:c.586T>C ENSP00000457737.1:p.Tyr196His
NM_001080442.2:c.586T>C NP_001073911.1:p.Tyr196His
XM_011522872.1:c.586T>C XP_011521174.1:p.Tyr196His
XM_017022946.1:c.586T>C XP_016878435.1:p.Tyr196His
NM_001080442.3:c.586T>C MANE Select NP_001073911.1:p.Tyr196His