Canonical Allele Identifier: CA802930345
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs1257283820
MyVariant Identifiers: chr5:g.1213503_1213504insC (hg19) chr5:g.1213388_1213389insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213393dup , CM000667.2:g.1213393dup GRCh38
NC_000005.9:g.1213508dup , CM000667.1:g.1213508dup GRCh37
NC_000005.8:g.1266508dup NCBI36
NG_008282.1:g.16799dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-70dup MANE Select ENSP00000305302.10:n.664-70dup
ENST00000304460.10:c.664-70dup ENSP00000305302.10:n.664-70dup
ENST00000515652.5:c.572-70dup ENSP00000425701.1:n.572-70dup
NM_001003841.2:c.664-70dup NP_001003841.1:n.664-70dup
NM_001003841.3:c.664-70dup MANE Select NP_001003841.1:n.664-70dup
Search 100 bp 5'
Search 100 bp 3'