Canonical Allele Identifier: CA3182846
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs747155465
gnomAD v2: 5-1213637-C-T
gnomAD v4: 5-1213522-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213522C>T , CM000667.2:g.1213522C>T GRCh38
NC_000005.9:g.1213637C>T , CM000667.1:g.1213637C>T GRCh37
NC_000005.8:g.1266637C>T NCBI36
NG_008282.1:g.16928C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.723C>T MANE Select ENSP00000305302.10:p.Gly241=
ENST00000304460.10:c.723C>T ENSP00000305302.10:p.Gly241=
ENST00000515652.5:c.631C>T ENSP00000425701.1:p.Pro211Ser
NM_001003841.2:c.723C>T NP_001003841.1:p.Gly241=
NM_001003841.3:c.723C>T MANE Select NP_001003841.1:p.Gly241=