Canonical Allele Identifier: CA145250792
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs938046238
gnomAD v2: 6-111544231-G-A
gnomAD v3: 6-111223028-G-A
gnomAD v4: 6-111223028-G-A
MyVariant Identifiers: chr6:g.111544231G>A (hg19) chr6:g.111223028G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111223028G>A , CM000668.2:g.111223028G>A GRCh38
NC_000006.11:g.111544231G>A , CM000668.1:g.111544231G>A GRCh37
NC_000006.10:g.111650924G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*793G>A MANE Select ENSP00000357844.4:n.*793G>A
ENST00000368850.4:c.*793G>A ENSP00000357843.1:n.*793G>A
NM_018593.4:c.*793G>A NP_061063.2:n.*793G>A
XM_017010237.1:c.*793G>A XP_016865726.1:n.*793G>A
XR_001743158.1:n.2623G>A
NM_018593.5:c.*793G>A MANE Select NP_061063.2:n.*793G>A
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