Canonical Allele Identifier: CA3182874
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs374898421
gnomAD v2: 5-1213715-C-T
gnomAD v3: 5-1213600-C-T
gnomAD v4: 5-1213600-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213600C>T , CM000667.2:g.1213600C>T GRCh38
NC_000005.9:g.1213715C>T , CM000667.1:g.1213715C>T GRCh37
NC_000005.8:g.1266715C>T NCBI36
NG_008282.1:g.17006C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.774+27C>T MANE Select ENSP00000305302.10:n.774+27C>T
ENST00000304460.10:c.774+27C>T ENSP00000305302.10:n.774+27C>T
ENST00000515652.5:c.682+27C>T ENSP00000425701.1:n.682+27C>T
NM_001003841.2:c.774+27C>T NP_001003841.1:n.774+27C>T
NM_001003841.3:c.774+27C>T MANE Select NP_001003841.1:n.774+27C>T