Canonical Allele Identifier: CA1522519782
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213222C= , CM000667.2:g.1213222C= GRCh38
NC_000005.9:g.1213337C= , CM000667.1:g.1213337C= GRCh37
NC_000005.8:g.1266337C= NCBI36
NG_008282.1:g.16628C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-241C= MANE Select ENSP00000305302.10:n.664-241C=
ENST00000304460.10:c.664-241C= ENSP00000305302.10:n.664-241C=
ENST00000515652.5:c.572-241C= ENSP00000425701.1:n.572-241C=
NM_001003841.2:c.664-241C= NP_001003841.1:n.664-241C=
NM_001003841.3:c.664-241C= MANE Select NP_001003841.1:n.664-241C=