Canonical Allele Identifier: CA1522520148
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213420C= , CM000667.2:g.1213420C= GRCh38
NC_000005.9:g.1213535C= , CM000667.1:g.1213535C= GRCh37
NC_000005.8:g.1266535C= NCBI36
NG_008282.1:g.16826C=

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.664-43C= MANE Select ENSP00000305302.10:n.664-43C=
ENST00000304460.10:c.664-43C= ENSP00000305302.10:n.664-43C=
ENST00000515652.5:c.572-43C= ENSP00000425701.1:n.572-43C=
NM_001003841.2:c.664-43C= NP_001003841.1:n.664-43C=
NM_001003841.3:c.664-43C= MANE Select NP_001003841.1:n.664-43C=