Canonical Allele Identifier: CA112941792
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs59928668
gnomAD v2: 5-1213833-C-A
gnomAD v3: 5-1213718-C-A
gnomAD v4: 5-1213718-C-A
MyVariant Identifiers: chr5:g.1213833C>A (hg19) chr5:g.1213718C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213718C>A , CM000667.2:g.1213718C>A GRCh38
NC_000005.9:g.1213833C>A , CM000667.1:g.1213833C>A GRCh37
NC_000005.8:g.1266833C>A NCBI36
NG_008282.1:g.17124C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.774+145C>A MANE Select ENSP00000305302.10:n.774+145C>A
ENST00000304460.10:c.774+145C>A ENSP00000305302.10:n.774+145C>A
ENST00000515652.5:c.682+145C>A ENSP00000425701.1:n.682+145C>A
NM_001003841.2:c.774+145C>A NP_001003841.1:n.774+145C>A
NM_001003841.3:c.774+145C>A MANE Select NP_001003841.1:n.774+145C>A
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