Canonical Allele Identifier: CA1522520473
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213645A= , CM000667.2:g.1213645A= GRCh38
NC_000005.9:g.1213760A= , CM000667.1:g.1213760A= GRCh37
NC_000005.8:g.1266760A= NCBI36
NG_008282.1:g.17051A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.774+72A= MANE Select ENSP00000305302.10:n.774+72A=
ENST00000304460.10:c.774+72A= ENSP00000305302.10:n.774+72A=
ENST00000515652.5:c.682+72A= ENSP00000425701.1:n.682+72A=
NM_001003841.2:c.774+72A= NP_001003841.1:n.774+72A=
NM_001003841.3:c.774+72A= MANE Select NP_001003841.1:n.774+72A=