Canonical Allele Identifier: CA2634582708
Gene: SLC38A8 HGNC NCBI

Linked Data

gnomAD v4: 16-84031816-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031816C>T , CM000678.2:g.84031816C>T GRCh38
NC_000016.9:g.84065421C>T , CM000678.1:g.84065421C>T GRCh37
NC_000016.8:g.82622922C>T NCBI36
NG_034136.1:g.15342G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299709.8:c.632+51G>A MANE Select ENSP00000299709.3:n.632+51G>A
ENST00000299709.7:c.632+51G>A ENSP00000299709.3:n.632+51G>A
ENST00000568178.1:c.632+51G>A ENSP00000457737.1:n.632+51G>A
NM_001080442.2:c.632+51G>A NP_001073911.1:n.632+51G>A
XM_011522872.1:c.632+51G>A XP_011521174.1:n.632+51G>A
XM_017022946.1:c.632+51G>A XP_016878435.1:n.632+51G>A
NM_001080442.3:c.632+51G>A MANE Select NP_001073911.1:n.632+51G>A
Search 100 bp 5'
Search 100 bp 3'