Canonical Allele Identifier: CA1522519779
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213220T= , CM000667.2:g.1213220T= GRCh38
NC_000005.9:g.1213335T= , CM000667.1:g.1213335T= GRCh37
NC_000005.8:g.1266335T= NCBI36
NG_008282.1:g.16626T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-243T= MANE Select ENSP00000305302.10:n.664-243T=
ENST00000304460.10:c.664-243T= ENSP00000305302.10:n.664-243T=
ENST00000515652.5:c.572-243T= ENSP00000425701.1:n.572-243T=
NM_001003841.2:c.664-243T= NP_001003841.1:n.664-243T=
NM_001003841.3:c.664-243T= MANE Select NP_001003841.1:n.664-243T=