Canonical Allele Identifier: CA359067628
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213524T>A , CM000667.2:g.1213524T>A GRCh38
NC_000005.9:g.1213639T>A , CM000667.1:g.1213639T>A GRCh37
NC_000005.8:g.1266639T>A NCBI36
NG_008282.1:g.16930T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.725T>A MANE Select ENSP00000305302.10:p.Leu242Gln
ENST00000304460.10:c.725T>A ENSP00000305302.10:p.Leu242Gln
ENST00000515652.5:c.633T>A ENSP00000425701.1:p.Pro211=
NM_001003841.2:c.725T>A NP_001003841.1:p.Leu242Gln
NM_001003841.3:c.725T>A MANE Select NP_001003841.1:p.Leu242Gln