Canonical Allele Identifier: CA359067609
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213521G>C , CM000667.2:g.1213521G>C GRCh38
NC_000005.9:g.1213636G>C , CM000667.1:g.1213636G>C GRCh37
NC_000005.8:g.1266636G>C NCBI36
NG_008282.1:g.16927G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.722G>C MANE Select ENSP00000305302.10:p.Gly241Ala
ENST00000304460.10:c.722G>C ENSP00000305302.10:p.Gly241Ala
ENST00000515652.5:c.630G>C ENSP00000425701.1:p.Arg210Ser
NM_001003841.2:c.722G>C NP_001003841.1:p.Gly241Ala
NM_001003841.3:c.722G>C MANE Select NP_001003841.1:p.Gly241Ala