Canonical Allele Identifier: CA1522519629
Gene: SLC6A19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213098C= , CM000667.2:g.1213098C= GRCh38
NC_000005.9:g.1213213C= , CM000667.1:g.1213213C= GRCh37
NC_000005.8:g.1266213C= NCBI36
NG_008282.1:g.16504C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-365C= MANE Select ENSP00000305302.10:n.664-365C=
ENST00000304460.10:c.664-365C= ENSP00000305302.10:n.664-365C=
ENST00000515652.5:c.572-365C= ENSP00000425701.1:n.572-365C=
NM_001003841.2:c.664-365C= NP_001003841.1:n.664-365C=
NM_001003841.3:c.664-365C= MANE Select NP_001003841.1:n.664-365C=
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