Canonical Allele Identifier: CA1522520031
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs1746103432

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213362C>T , CM000667.2:g.1213362C>T GRCh38
NC_000005.9:g.1213477C>T , CM000667.1:g.1213477C>T GRCh37
NC_000005.8:g.1266477C>T NCBI36
NG_008282.1:g.16768C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-101C>T MANE Select ENSP00000305302.10:n.664-101C>T
ENST00000304460.10:c.664-101C>T ENSP00000305302.10:n.664-101C>T
ENST00000515652.5:c.572-101C>T ENSP00000425701.1:n.572-101C>T
NM_001003841.2:c.664-101C>T NP_001003841.1:n.664-101C>T
NM_001003841.3:c.664-101C>T MANE Select NP_001003841.1:n.664-101C>T