Canonical Allele Identifier: CA359067582
Gene: SLC6A19 HGNC NCBI

Linked Data

gnomAD v4: 5-1213517-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213517C>G , CM000667.2:g.1213517C>G GRCh38
NC_000005.9:g.1213632C>G , CM000667.1:g.1213632C>G GRCh37
NC_000005.8:g.1266632C>G NCBI36
NG_008282.1:g.16923C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.718C>G MANE Select ENSP00000305302.10:p.Arg240Gly
ENST00000304460.10:c.718C>G ENSP00000305302.10:p.Arg240Gly
ENST00000515652.5:c.626C>G ENSP00000425701.1:p.Pro209Arg
NM_001003841.2:c.718C>G NP_001003841.1:p.Arg240Gly
NM_001003841.3:c.718C>G MANE Select NP_001003841.1:p.Arg240Gly