Canonical Allele Identifier: CA1522519801
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213235A= , CM000667.2:g.1213235A= GRCh38
NC_000005.9:g.1213350A= , CM000667.1:g.1213350A= GRCh37
NC_000005.8:g.1266350A= NCBI36
NG_008282.1:g.16641A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-228A= MANE Select ENSP00000305302.10:n.664-228A=
ENST00000304460.10:c.664-228A= ENSP00000305302.10:n.664-228A=
ENST00000515652.5:c.572-228A= ENSP00000425701.1:n.572-228A=
NM_001003841.2:c.664-228A= NP_001003841.1:n.664-228A=
NM_001003841.3:c.664-228A= MANE Select NP_001003841.1:n.664-228A=