Canonical Allele Identifier: CA443019117
Gene: SLC6A19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1213637C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213522C>A , CM000667.2:g.1213522C>A GRCh38
NC_000005.9:g.1213637C>A , CM000667.1:g.1213637C>A GRCh37
NC_000005.8:g.1266637C>A NCBI36
NG_008282.1:g.16928C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.723C>A MANE Select ENSP00000305302.10:p.Gly241=
ENST00000304460.10:c.723C>A ENSP00000305302.10:p.Gly241=
ENST00000515652.5:c.631C>A ENSP00000425701.1:p.Pro211Thr
NM_001003841.2:c.723C>A NP_001003841.1:p.Gly241=
NM_001003841.3:c.723C>A MANE Select NP_001003841.1:p.Gly241=