Canonical Allele Identifier: CA359067607
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213521G>A , CM000667.2:g.1213521G>A GRCh38
NC_000005.9:g.1213636G>A , CM000667.1:g.1213636G>A GRCh37
NC_000005.8:g.1266636G>A NCBI36
NG_008282.1:g.16927G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.722G>A MANE Select ENSP00000305302.10:p.Gly241Asp
ENST00000304460.10:c.722G>A ENSP00000305302.10:p.Gly241Asp
ENST00000515652.5:c.630G>A ENSP00000425701.1:p.Arg210=
NM_001003841.2:c.722G>A NP_001003841.1:p.Gly241Asp
NM_001003841.3:c.722G>A MANE Select NP_001003841.1:p.Gly241Asp