Canonical Allele Identifier: CA413655928
Gene: SLC16A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73641644C>G (hg19) chrX:g.74421809C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421809C>G , CM000685.2:g.74421809C>G GRCh38
NC_000023.10:g.73641644C>G , CM000685.1:g.73641644C>G GRCh37
NC_000023.9:g.73558369C>G NCBI36
NG_011641.1:g.5560C>G
NG_011641.2:g.5560C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.172C>G MANE Select ENSP00000465734.1:p.Leu58Val
ENST00000587091.5:c.172C>G ENSP00000465734.1:p.Leu58Val
NM_006517.4:c.172C>G NP_006508.2:p.Leu58Val
XM_005262294.1:c.172C>G XP_005262351.1:p.Leu58Val
XM_011531015.1:c.172C>G XP_011529317.1:p.Leu58Val
NM_006517.5:c.172C>G MANE Select NP_006508.2:p.Leu58Val
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