Canonical Allele Identifier: CA396938406
Gene: SLC38A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031879T>C , CM000678.2:g.84031879T>C GRCh38
NC_000016.9:g.84065484T>C , CM000678.1:g.84065484T>C GRCh37
NC_000016.8:g.82622985T>C NCBI36
NG_034136.1:g.15279A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.620A>G MANE Select ENSP00000299709.3:p.His207Arg
ENST00000299709.7:c.620A>G ENSP00000299709.3:p.His207Arg
ENST00000568178.1:c.620A>G ENSP00000457737.1:p.His207Arg
NM_001080442.2:c.620A>G NP_001073911.1:p.His207Arg
XM_011522872.1:c.620A>G XP_011521174.1:p.His207Arg
XM_017022946.1:c.620A>G XP_016878435.1:p.His207Arg
NM_001080442.3:c.620A>G MANE Select NP_001073911.1:p.His207Arg