Canonical Allele Identifier: CA1522520753
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213895C= , CM000667.2:g.1213895C= GRCh38
NC_000005.9:g.1214010C= , CM000667.1:g.1214010C= GRCh37
NC_000005.8:g.1267010C= NCBI36
NG_008282.1:g.17301C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.775-58C= MANE Select ENSP00000305302.10:n.775-58C=
ENST00000304460.10:c.775-58C= ENSP00000305302.10:n.775-58C=
ENST00000515652.5:c.683-58C= ENSP00000425701.1:n.683-58C=
NM_001003841.2:c.775-58C= NP_001003841.1:n.775-58C=
NM_001003841.3:c.775-58C= MANE Select NP_001003841.1:n.775-58C=