Canonical Allele Identifier: CA359067733
Gene: SLC6A19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1213665A>C (hg19) chr5:g.1213550A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213550A>C , CM000667.2:g.1213550A>C GRCh38
NC_000005.9:g.1213665A>C , CM000667.1:g.1213665A>C GRCh37
NC_000005.8:g.1266665A>C NCBI36
NG_008282.1:g.16956A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.751A>C MANE Select ENSP00000305302.10:p.Ile251Leu
ENST00000304460.10:c.751A>C ENSP00000305302.10:p.Ile251Leu
ENST00000515652.5:c.659A>C ENSP00000425701.1:p.His220Pro
NM_001003841.2:c.751A>C NP_001003841.1:p.Ile251Leu
NM_001003841.3:c.751A>C MANE Select NP_001003841.1:p.Ile251Leu
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