Canonical Allele Identifier: CA517243043
Gene: SLC16A2 HGNC NCBI

Linked Data

dbSNP Id: rs2147871891
MyVariant Identifiers: chrX:g.73749200A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529365A>T , CM000685.2:g.74529365A>T GRCh38
NC_000023.10:g.73749200A>T , CM000685.1:g.73749200A>T GRCh37
NC_000023.9:g.73665925A>T NCBI36
NG_011641.1:g.113116A>T
NG_011641.2:g.113116A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1323A>T MANE Select ENSP00000465734.1:p.Pro441=
ENST00000636771.1:c.1232A>T
ENST00000587091.5:c.1323A>T ENSP00000465734.1:p.Pro441=
ENST00000590447.1:c.611-1968A>T
NM_006517.4:c.1323A>T NP_006508.2:p.Pro441=
XM_005262294.1:c.1171-1968A>T XP_005262351.1:n.1171-1968A>T
NM_006517.5:c.1323A>T MANE Select NP_006508.2:p.Pro441=