Canonical Allele Identifier: CA415077745
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 940774
ClinVar RCV Id: RCV001210427
dbSNP Id: rs2091449037

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153690454G>C , CM000685.2:g.153690454G>C GRCh38
NC_000023.10:g.152955909G>C , CM000685.1:g.152955909G>C GRCh37
NC_000023.9:g.152609103G>C NCBI36
NG_012016.1:g.7158G>C
NG_012016.2:g.7158G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.342G>C MANE Select ENSP00000253122.5:p.Gln114His
ENST00000675713.1:n.96G>C
ENST00000253122.9:c.342G>C ENSP00000253122.5:p.Gln114His
ENST00000430077.6:c.-4G>C ENSP00000403041.2:n.-4G>C
ENST00000476466.1:n.194G>C
NM_001142805.1:c.342G>C NP_001136277.1:p.Gln114His
NM_001142806.1:c.-4G>C NP_001136278.1:n.-4G>C
NM_005629.3:c.342G>C NP_005620.1:p.Gln114His
NM_005629.4:c.342G>C MANE Select NP_005620.1:p.Gln114His
NM_001142805.2:c.342G>C NP_001136277.1:p.Gln114His