Canonical Allele Identifier: CA396938816
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs1181417797

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031957G>C , CM000678.2:g.84031957G>C GRCh38
NC_000016.9:g.84065562G>C , CM000678.1:g.84065562G>C GRCh37
NC_000016.8:g.82623063G>C NCBI36
NG_034136.1:g.15201C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.542C>G MANE Select ENSP00000299709.3:p.Thr181Ser
ENST00000299709.7:c.542C>G ENSP00000299709.3:p.Thr181Ser
ENST00000568178.1:c.542C>G ENSP00000457737.1:p.Thr181Ser
NM_001080442.2:c.542C>G NP_001073911.1:p.Thr181Ser
XM_011522872.1:c.542C>G XP_011521174.1:p.Thr181Ser
XM_017022946.1:c.542C>G XP_016878435.1:p.Thr181Ser
NM_001080442.3:c.542C>G MANE Select NP_001073911.1:p.Thr181Ser