Canonical Allele Identifier: CA145250789
Gene: SLC16A10 HGNC NCBI

Linked Data

dbSNP Id: rs534538314
gnomAD v3: 6-111223017-G-T
gnomAD v4: 6-111223017-G-T
MyVariant Identifiers: chr6:g.111544220G>T (hg19) chr6:g.111223017G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111223017G>T , CM000668.2:g.111223017G>T GRCh38
NC_000006.11:g.111544220G>T , CM000668.1:g.111544220G>T GRCh37
NC_000006.10:g.111650913G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368851.10:c.*782G>T MANE Select ENSP00000357844.4:n.*782G>T
ENST00000368850.4:c.*782G>T ENSP00000357843.1:n.*782G>T
ENST00000368851.9:c.*782G>T ENSP00000357844.4:n.*782G>T
NM_018593.4:c.*782G>T NP_061063.2:n.*782G>T
XM_005266818.2:c.*736G>T XP_005266875.1:n.*736G>T
XM_017010237.1:c.*782G>T XP_016865726.1:n.*782G>T
XR_001743158.1:n.2612G>T
NM_018593.5:c.*782G>T MANE Select NP_061063.2:n.*782G>T
Search 100 bp 5'
Search 100 bp 3'