Canonical Allele Identifier: CA1522520271
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213503C= , CM000667.2:g.1213503C= GRCh38
NC_000005.9:g.1213618C= , CM000667.1:g.1213618C= GRCh37
NC_000005.8:g.1266618C= NCBI36
NG_008282.1:g.16909C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.704C= MANE Select ENSP00000305302.10:p.Thr235=
ENST00000304460.10:c.704C= ENSP00000305302.10:p.Thr235=
ENST00000515652.5:c.612C= ENSP00000425701.1:p.Asp204=
NM_001003841.2:c.704C= NP_001003841.1:p.Thr235=
NM_001003841.3:c.704C= MANE Select NP_001003841.1:p.Thr235=