Canonical Allele Identifier: CA1522520242
Gene: SLC6A19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213476C= , CM000667.2:g.1213476C= GRCh38
NC_000005.9:g.1213591C= , CM000667.1:g.1213591C= GRCh37
NC_000005.8:g.1266591C= NCBI36
NG_008282.1:g.16882C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.677C= MANE Select ENSP00000305302.10:p.Thr226=
ENST00000304460.10:c.677C= ENSP00000305302.10:p.Thr226=
ENST00000515652.5:c.585C= ENSP00000425701.1:p.His195=
NM_001003841.2:c.677C= NP_001003841.1:p.Thr226=
NM_001003841.3:c.677C= MANE Select NP_001003841.1:p.Thr226=
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