Canonical Allele Identifier: CA1522518600
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212248T= , CM000667.2:g.1212248T= GRCh38
NC_000005.9:g.1212363T= , CM000667.1:g.1212363T= GRCh37
NC_000005.8:g.1265363T= NCBI36
NG_008282.1:g.15654T=

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.482-55T= MANE Select ENSP00000305302.10:n.482-55T=
ENST00000304460.10:c.482-55T= ENSP00000305302.10:n.482-55T=
ENST00000515652.5:c.390-55T= ENSP00000425701.1:n.390-55T=
NM_001003841.2:c.482-55T= NP_001003841.1:n.482-55T=
NM_001003841.3:c.482-55T= MANE Select NP_001003841.1:n.482-55T=