Canonical Allele Identifier: CA569615086
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs1366962557
gnomAD v2: 6-111544226-C-T
gnomAD v3: 6-111223023-C-T
gnomAD v4: 6-111223023-C-T
MyVariant Identifiers: chr6:g.111544226C>T (hg19) chr6:g.111223023C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111223023C>T , CM000668.2:g.111223023C>T GRCh38
NC_000006.11:g.111544226C>T , CM000668.1:g.111544226C>T GRCh37
NC_000006.10:g.111650919C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*788C>T MANE Select ENSP00000357844.4:n.*788C>T
ENST00000368850.4:c.*788C>T ENSP00000357843.1:n.*788C>T
NM_018593.4:c.*788C>T NP_061063.2:n.*788C>T
XM_017010237.1:c.*788C>T XP_016865726.1:n.*788C>T
XR_001743158.1:n.2618C>T
NM_018593.5:c.*788C>T MANE Select NP_061063.2:n.*788C>T
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