Canonical Allele Identifier: CA2437508404
Gene: SLC16A2 HGNC NCBI

Linked Data

dbSNP Id: rs1930476660
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525662A>C , CM000685.2:g.74525662A>C GRCh38
NC_000023.10:g.73745497A>C , CM000685.1:g.73745497A>C GRCh37
NC_000023.9:g.73662222A>C NCBI36
NG_011641.1:g.109413A>C
NG_011641.2:g.109413A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.1027-88A>C MANE Select ENSP00000465734.1:n.1027-88A>C
ENST00000636771.1:c.936-88A>C
ENST00000587091.5:c.1027-88A>C ENSP00000465734.1:n.1027-88A>C
ENST00000590447.1:c.467-88A>C
NM_006517.4:c.1027-88A>C NP_006508.2:n.1027-88A>C
XM_005262294.1:c.1027-88A>C XP_005262351.1:n.1027-88A>C
XM_011531015.1:c.*31-88A>C XP_011529317.1:n.*31-88A>C
NM_006517.5:c.1027-88A>C MANE Select NP_006508.2:n.1027-88A>C
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