Canonical Allele Identifier: CA1522520235
Gene: SLC6A19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213472A= , CM000667.2:g.1213472A= GRCh38
NC_000005.9:g.1213587A= , CM000667.1:g.1213587A= GRCh37
NC_000005.8:g.1266587A= NCBI36
NG_008282.1:g.16878A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.673A= MANE Select ENSP00000305302.10:p.Ile225=
ENST00000304460.10:c.673A= ENSP00000305302.10:p.Ile225=
ENST00000515652.5:c.581A= ENSP00000425701.1:p.His194=
NM_001003841.2:c.673A= NP_001003841.1:p.Ile225=
NM_001003841.3:c.673A= MANE Select NP_001003841.1:p.Ile225=
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