Canonical Allele Identifier: CA3182876
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs201708436
gnomAD v2: 5-1213719-C-A
gnomAD v3: 5-1213604-C-A
gnomAD v4: 5-1213604-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213604C>A , CM000667.2:g.1213604C>A GRCh38
NC_000005.9:g.1213719C>A , CM000667.1:g.1213719C>A GRCh37
NC_000005.8:g.1266719C>A NCBI36
NG_008282.1:g.17010C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.774+31C>A MANE Select ENSP00000305302.10:n.774+31C>A
ENST00000304460.10:c.774+31C>A ENSP00000305302.10:n.774+31C>A
ENST00000515652.5:c.682+31C>A ENSP00000425701.1:n.682+31C>A
NM_001003841.2:c.774+31C>A NP_001003841.1:n.774+31C>A
NM_001003841.3:c.774+31C>A MANE Select NP_001003841.1:n.774+31C>A