Canonical Allele Identifier: CA413656277
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74421975-C-G
MyVariant Identifiers: chrX:g.73641810C>G (hg19) chrX:g.74421975C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421975C>G , CM000685.2:g.74421975C>G GRCh38
NC_000023.10:g.73641810C>G , CM000685.1:g.73641810C>G GRCh37
NC_000023.9:g.73558535C>G NCBI36
NG_011641.1:g.5726C>G
NG_011641.2:g.5726C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.338C>G MANE Select ENSP00000465734.1:p.Ser113Cys
ENST00000636771.1:c.84C>G
ENST00000587091.5:c.338C>G ENSP00000465734.1:p.Ser113Cys
NM_006517.4:c.338C>G NP_006508.2:p.Ser113Cys
XM_005262294.1:c.338C>G XP_005262351.1:p.Ser113Cys
XM_011531015.1:c.338C>G XP_011529317.1:p.Ser113Cys
NM_006517.5:c.338C>G MANE Select NP_006508.2:p.Ser113Cys
Search 100 bp 5'
Search 100 bp 3'