Canonical Allele Identifier: CA1522518592
Gene: SLC6A19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212239G= , CM000667.2:g.1212239G= GRCh38
NC_000005.9:g.1212354G= , CM000667.1:g.1212354G= GRCh37
NC_000005.8:g.1265354G= NCBI36
NG_008282.1:g.15645G=

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.482-64G= MANE Select ENSP00000305302.10:n.482-64G=
ENST00000304460.10:c.482-64G= ENSP00000305302.10:n.482-64G=
ENST00000515652.5:c.390-64G= ENSP00000425701.1:n.390-64G=
NM_001003841.2:c.482-64G= NP_001003841.1:n.482-64G=
NM_001003841.3:c.482-64G= MANE Select NP_001003841.1:n.482-64G=
Search 100 bp 5'
Search 100 bp 3'