Canonical Allele Identifier: CA2765038626
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213050G>T , CM000667.2:g.1213050G>T GRCh38
NC_000005.9:g.1213165G>T , CM000667.1:g.1213165G>T GRCh37
NC_000005.8:g.1266165G>T NCBI36
NG_008282.1:g.16456G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-413G>T MANE Select ENSP00000305302.10:n.664-413G>T
ENST00000304460.10:c.664-413G>T ENSP00000305302.10:n.664-413G>T
ENST00000515652.5:c.572-413G>T ENSP00000425701.1:n.572-413G>T
NM_001003841.2:c.664-413G>T NP_001003841.1:n.664-413G>T
NM_001003841.3:c.664-413G>T MANE Select NP_001003841.1:n.664-413G>T