Canonical Allele Identifier: CA817165783
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs1202394841
gnomAD v3: 6-111222671-T-C
gnomAD v4: 6-111222671-T-C
MyVariant Identifiers: chr6:g.111543874T>C (hg19) chr6:g.111222671T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222671T>C , CM000668.2:g.111222671T>C GRCh38
NC_000006.11:g.111543874T>C , CM000668.1:g.111543874T>C GRCh37
NC_000006.10:g.111650567T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368851.10:c.*436T>C MANE Select ENSP00000357844.4:n.*436T>C
ENST00000368850.4:c.*436T>C ENSP00000357843.1:n.*436T>C
ENST00000368851.9:c.*436T>C ENSP00000357844.4:n.*436T>C
NM_018593.4:c.*436T>C NP_061063.2:n.*436T>C
XM_005266818.2:c.*390T>C XP_005266875.1:n.*390T>C
XM_017010237.1:c.*436T>C XP_016865726.1:n.*436T>C
XR_001743158.1:n.2266T>C
NM_018593.5:c.*436T>C MANE Select NP_061063.2:n.*436T>C
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