Canonical Allele Identifier: CA1522519601
Gene: SLC6A19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213056C= , CM000667.2:g.1213056C= GRCh38
NC_000005.9:g.1213171C= , CM000667.1:g.1213171C= GRCh37
NC_000005.8:g.1266171C= NCBI36
NG_008282.1:g.16462C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-407C= MANE Select ENSP00000305302.10:n.664-407C=
ENST00000304460.10:c.664-407C= ENSP00000305302.10:n.664-407C=
ENST00000515652.5:c.572-407C= ENSP00000425701.1:n.572-407C=
NM_001003841.2:c.664-407C= NP_001003841.1:n.664-407C=
NM_001003841.3:c.664-407C= MANE Select NP_001003841.1:n.664-407C=
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