Canonical Allele Identifier: CA145250768
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs554958982
gnomAD v3: 6-111222924-G-A
gnomAD v4: 6-111222924-G-A
MyVariant Identifiers: chr6:g.111544127G>A (hg19) chr6:g.111222924G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111222924G>A , CM000668.2:g.111222924G>A GRCh38
NC_000006.11:g.111544127G>A , CM000668.1:g.111544127G>A GRCh37
NC_000006.10:g.111650820G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*689G>A MANE Select ENSP00000357844.4:n.*689G>A
ENST00000368850.4:c.*689G>A ENSP00000357843.1:n.*689G>A
ENST00000368851.9:c.*689G>A ENSP00000357844.4:n.*689G>A
NM_018593.4:c.*689G>A NP_061063.2:n.*689G>A
XM_005266818.2:c.*643G>A XP_005266875.1:n.*643G>A
XM_017010237.1:c.*689G>A XP_016865726.1:n.*689G>A
XR_001743158.1:n.2519G>A
NM_018593.5:c.*689G>A MANE Select NP_061063.2:n.*689G>A
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