Canonical Allele Identifier: CA1522520561
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213734C= , CM000667.2:g.1213734C= GRCh38
NC_000005.9:g.1213849C= , CM000667.1:g.1213849C= GRCh37
NC_000005.8:g.1266849C= NCBI36
NG_008282.1:g.17140C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.774+161C= MANE Select ENSP00000305302.10:n.774+161C=
ENST00000304460.10:c.774+161C= ENSP00000305302.10:n.774+161C=
ENST00000515652.5:c.682+161C= ENSP00000425701.1:n.682+161C=
NM_001003841.2:c.774+161C= NP_001003841.1:n.774+161C=
NM_001003841.3:c.774+161C= MANE Select NP_001003841.1:n.774+161C=