Canonical Allele Identifier: CA3182851
Gene: SLC6A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469821
ClinVar RCV Id: RCV002571269 RCV001973111
dbSNP Id: rs201050149
ExAC: 5:1213653 G / A
gnomAD v2: 5-1213653-G-A
gnomAD v3: 5-1213538-G-A
gnomAD v4: 5-1213538-G-A
MyVariant Identifiers: chr5:g.1213653G>A (hg19) chr5:g.1213538G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213538G>A , CM000667.2:g.1213538G>A GRCh38
NC_000005.9:g.1213653G>A , CM000667.1:g.1213653G>A GRCh37
NC_000005.8:g.1266653G>A NCBI36
NG_008282.1:g.16944G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.739G>A MANE Select ENSP00000305302.10:p.Ala247Thr
ENST00000304460.10:c.739G>A ENSP00000305302.10:p.Ala247Thr
ENST00000515652.5:c.647G>A ENSP00000425701.1:p.Arg216His
NM_001003841.2:c.739G>A NP_001003841.1:p.Ala247Thr
NM_001003841.3:c.739G>A MANE Select NP_001003841.1:p.Ala247Thr
Search 100 bp 5'
Search 100 bp 3'