Canonical Allele Identifier: CA112941222
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs543199799
gnomAD v2: 5-1213197-C-T
gnomAD v3: 5-1213082-C-T
gnomAD v4: 5-1213082-C-T
MyVariant Identifiers: chr5:g.1213197C>T (hg19) chr5:g.1213082C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213082C>T , CM000667.2:g.1213082C>T GRCh38
NC_000005.9:g.1213197C>T , CM000667.1:g.1213197C>T GRCh37
NC_000005.8:g.1266197C>T NCBI36
NG_008282.1:g.16488C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-381C>T MANE Select ENSP00000305302.10:n.664-381C>T
ENST00000304460.10:c.664-381C>T ENSP00000305302.10:n.664-381C>T
ENST00000515652.5:c.572-381C>T ENSP00000425701.1:n.572-381C>T
NM_001003841.2:c.664-381C>T NP_001003841.1:n.664-381C>T
NM_001003841.3:c.664-381C>T MANE Select NP_001003841.1:n.664-381C>T
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