Canonical Allele Identifier: CA1522520773
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213910C= , CM000667.2:g.1213910C= GRCh38
NC_000005.9:g.1214025C= , CM000667.1:g.1214025C= GRCh37
NC_000005.8:g.1267025C= NCBI36
NG_008282.1:g.17316C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.775-43C= MANE Select ENSP00000305302.10:n.775-43C=
ENST00000304460.10:c.775-43C= ENSP00000305302.10:n.775-43C=
ENST00000515652.5:c.683-43C= ENSP00000425701.1:n.683-43C=
NM_001003841.2:c.775-43C= NP_001003841.1:n.775-43C=
NM_001003841.3:c.775-43C= MANE Select NP_001003841.1:n.775-43C=