Canonical Allele Identifier: CA802930957
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs1364724943
MyVariant Identifiers: chr5:g.1213878G>C (hg19) chr5:g.1213763G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213763G>C , CM000667.2:g.1213763G>C GRCh38
NC_000005.9:g.1213878G>C , CM000667.1:g.1213878G>C GRCh37
NC_000005.8:g.1266878G>C NCBI36
NG_008282.1:g.17169G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.775-190G>C MANE Select ENSP00000305302.10:n.775-190G>C
ENST00000304460.10:c.775-190G>C ENSP00000305302.10:n.775-190G>C
ENST00000515652.5:c.683-190G>C ENSP00000425701.1:n.683-190G>C
NM_001003841.2:c.775-190G>C NP_001003841.1:n.775-190G>C
NM_001003841.3:c.775-190G>C MANE Select NP_001003841.1:n.775-190G>C
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