Canonical Allele Identifier: CA1522519751
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213202A= , CM000667.2:g.1213202A= GRCh38
NC_000005.9:g.1213317A= , CM000667.1:g.1213317A= GRCh37
NC_000005.8:g.1266317A= NCBI36
NG_008282.1:g.16608A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-261A= MANE Select ENSP00000305302.10:n.664-261A=
ENST00000304460.10:c.664-261A= ENSP00000305302.10:n.664-261A=
ENST00000515652.5:c.572-261A= ENSP00000425701.1:n.572-261A=
NM_001003841.2:c.664-261A= NP_001003841.1:n.664-261A=
NM_001003841.3:c.664-261A= MANE Select NP_001003841.1:n.664-261A=