Canonical Allele Identifier: CA359067669
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213534G>C , CM000667.2:g.1213534G>C GRCh38
NC_000005.9:g.1213649G>C , CM000667.1:g.1213649G>C GRCh37
NC_000005.8:g.1266649G>C NCBI36
NG_008282.1:g.16940G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.735G>C MANE Select ENSP00000305302.10:p.Lys245Asn
ENST00000304460.10:c.735G>C ENSP00000305302.10:p.Lys245Asn
ENST00000515652.5:c.643G>C ENSP00000425701.1:p.Gly215Arg
NM_001003841.2:c.735G>C NP_001003841.1:p.Lys245Asn
NM_001003841.3:c.735G>C MANE Select NP_001003841.1:p.Lys245Asn