Canonical Allele Identifier: CA2557012635
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213081C>T , CM000667.2:g.1213081C>T GRCh38
NC_000005.9:g.1213196C>T , CM000667.1:g.1213196C>T GRCh37
NC_000005.8:g.1266196C>T NCBI36
NG_008282.1:g.16487C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-382C>T MANE Select ENSP00000305302.10:n.664-382C>T
ENST00000304460.10:c.664-382C>T ENSP00000305302.10:n.664-382C>T
ENST00000515652.5:c.572-382C>T ENSP00000425701.1:n.572-382C>T
NM_001003841.2:c.664-382C>T NP_001003841.1:n.664-382C>T
NM_001003841.3:c.664-382C>T MANE Select NP_001003841.1:n.664-382C>T