Canonical Allele Identifier: CA1522520083
Gene: SLC6A19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213387C= , CM000667.2:g.1213387C= GRCh38
NC_000005.9:g.1213502C= , CM000667.1:g.1213502C= GRCh37
NC_000005.8:g.1266502C= NCBI36
NG_008282.1:g.16793C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-76C= MANE Select ENSP00000305302.10:n.664-76C=
ENST00000304460.10:c.664-76C= ENSP00000305302.10:n.664-76C=
ENST00000515652.5:c.572-76C= ENSP00000425701.1:n.572-76C=
NM_001003841.2:c.664-76C= NP_001003841.1:n.664-76C=
NM_001003841.3:c.664-76C= MANE Select NP_001003841.1:n.664-76C=
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