Canonical Allele Identifier: CA2694115169
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74525692-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525692A>G , CM000685.2:g.74525692A>G GRCh38
NC_000023.10:g.73745527A>G , CM000685.1:g.73745527A>G GRCh37
NC_000023.9:g.73662252A>G NCBI36
NG_011641.1:g.109443A>G
NG_011641.2:g.109443A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.1027-58A>G MANE Select ENSP00000465734.1:n.1027-58A>G
ENST00000636771.1:c.936-58A>G
ENST00000587091.5:c.1027-58A>G ENSP00000465734.1:n.1027-58A>G
ENST00000590447.1:c.467-58A>G
NM_006517.4:c.1027-58A>G NP_006508.2:n.1027-58A>G
XM_005262294.1:c.1027-58A>G XP_005262351.1:n.1027-58A>G
XM_011531015.1:c.*31-58A>G XP_011529317.1:n.*31-58A>G
NM_006517.5:c.1027-58A>G MANE Select NP_006508.2:n.1027-58A>G
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