Canonical Allele Identifier: CA359067699
Gene: SLC6A19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1213656A>T (hg19) chr5:g.1213541A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213541A>T , CM000667.2:g.1213541A>T GRCh38
NC_000005.9:g.1213656A>T , CM000667.1:g.1213656A>T GRCh37
NC_000005.8:g.1266656A>T NCBI36
NG_008282.1:g.16947A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.742A>T MANE Select ENSP00000305302.10:p.Thr248Ser
ENST00000304460.10:c.742A>T ENSP00000305302.10:p.Thr248Ser
ENST00000515652.5:c.650A>T ENSP00000425701.1:p.His217Leu
NM_001003841.2:c.742A>T NP_001003841.1:p.Thr248Ser
NM_001003841.3:c.742A>T MANE Select NP_001003841.1:p.Thr248Ser
Search 100 bp 5'
Search 100 bp 3'