Canonical Allele Identifier: CA359067604
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs1746112589

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213520G>T , CM000667.2:g.1213520G>T GRCh38
NC_000005.9:g.1213635G>T , CM000667.1:g.1213635G>T GRCh37
NC_000005.8:g.1266635G>T NCBI36
NG_008282.1:g.16926G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.721G>T MANE Select ENSP00000305302.10:p.Gly241Cys
ENST00000304460.10:c.721G>T ENSP00000305302.10:p.Gly241Cys
ENST00000515652.5:c.629G>T ENSP00000425701.1:p.Arg210Met
NM_001003841.2:c.721G>T NP_001003841.1:p.Gly241Cys
NM_001003841.3:c.721G>T MANE Select NP_001003841.1:p.Gly241Cys