Canonical Allele Identifier: CA1522519515
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs1746086312

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212969G>T , CM000667.2:g.1212969G>T GRCh38
NC_000005.9:g.1213084G>T , CM000667.1:g.1213084G>T GRCh37
NC_000005.8:g.1266084G>T NCBI36
NG_008282.1:g.16375G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.663+485G>T MANE Select ENSP00000305302.10:n.663+485G>T
ENST00000304460.10:c.663+485G>T ENSP00000305302.10:n.663+485G>T
ENST00000515652.5:c.571+485G>T ENSP00000425701.1:n.571+485G>T
NM_001003841.2:c.663+485G>T NP_001003841.1:n.663+485G>T
NM_001003841.3:c.663+485G>T MANE Select NP_001003841.1:n.663+485G>T