Canonical Allele Identifier: CA1522519529
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs1746086688

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212976C>G , CM000667.2:g.1212976C>G GRCh38
NC_000005.9:g.1213091C>G , CM000667.1:g.1213091C>G GRCh37
NC_000005.8:g.1266091C>G NCBI36
NG_008282.1:g.16382C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-487C>G MANE Select ENSP00000305302.10:n.664-487C>G
ENST00000304460.10:c.664-487C>G ENSP00000305302.10:n.664-487C>G
ENST00000515652.5:c.572-487C>G ENSP00000425701.1:n.572-487C>G
NM_001003841.2:c.664-487C>G NP_001003841.1:n.664-487C>G
NM_001003841.3:c.664-487C>G MANE Select NP_001003841.1:n.664-487C>G