Canonical Allele Identifier: CA517464419
Gene: SLC16A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73641808C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421973C>G , CM000685.2:g.74421973C>G GRCh38
NC_000023.10:g.73641808C>G , CM000685.1:g.73641808C>G GRCh37
NC_000023.9:g.73558533C>G NCBI36
NG_011641.1:g.5724C>G
NG_011641.2:g.5724C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.336C>G MANE Select ENSP00000465734.1:p.Gly112=
ENST00000636771.1:c.82C>G
ENST00000587091.5:c.336C>G ENSP00000465734.1:p.Gly112=
NM_006517.4:c.336C>G NP_006508.2:p.Gly112=
XM_005262294.1:c.336C>G XP_005262351.1:p.Gly112=
XM_011531015.1:c.336C>G XP_011529317.1:p.Gly112=
NM_006517.5:c.336C>G MANE Select NP_006508.2:p.Gly112=
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