Canonical Allele Identifier: CA2673072374
Gene: SLC6A19 HGNC NCBI

Linked Data

gnomAD v4: 5-1213682-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213682G>A , CM000667.2:g.1213682G>A GRCh38
NC_000005.9:g.1213797G>A , CM000667.1:g.1213797G>A GRCh37
NC_000005.8:g.1266797G>A NCBI36
NG_008282.1:g.17088G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.774+109G>A MANE Select ENSP00000305302.10:n.774+109G>A
ENST00000304460.10:c.774+109G>A ENSP00000305302.10:n.774+109G>A
ENST00000515652.5:c.682+109G>A ENSP00000425701.1:n.682+109G>A
NM_001003841.2:c.774+109G>A NP_001003841.1:n.774+109G>A
NM_001003841.3:c.774+109G>A MANE Select NP_001003841.1:n.774+109G>A
Search 100 bp 5'
Search 100 bp 3'