Canonical Allele Identifier: CA517244178
Gene: SLC16A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73751172A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74531337A>G , CM000685.2:g.74531337A>G GRCh38
NC_000023.10:g.73751172A>G , CM000685.1:g.73751172A>G GRCh37
NC_000023.9:g.73667897A>G NCBI36
NG_011641.1:g.115088A>G
NG_011641.2:g.115088A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.1404A>G MANE Select ENSP00000465734.1:p.Leu468=
ENST00000636771.1:c.1313A>G
ENST00000587091.5:c.1404A>G ENSP00000465734.1:p.Leu468=
ENST00000590447.1:c.615A>G
NM_006517.4:c.1404A>G NP_006508.2:p.Leu468=
XM_005262294.1:c.1175A>G XP_005262351.1:p.Tyr392Cys
NM_006517.5:c.1404A>G MANE Select NP_006508.2:p.Leu468=