Canonical Allele Identifier: CA517464413
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74421967-C-T
MyVariant Identifiers: chrX:g.73641802C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421967C>T , CM000685.2:g.74421967C>T GRCh38
NC_000023.10:g.73641802C>T , CM000685.1:g.73641802C>T GRCh37
NC_000023.9:g.73558527C>T NCBI36
NG_011641.1:g.5718C>T
NG_011641.2:g.5718C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.330C>T MANE Select ENSP00000465734.1:p.Cys110=
ENST00000636771.1:c.76C>T
ENST00000587091.5:c.330C>T ENSP00000465734.1:p.Cys110=
NM_006517.4:c.330C>T NP_006508.2:p.Cys110=
XM_005262294.1:c.330C>T XP_005262351.1:p.Cys110=
XM_011531015.1:c.330C>T XP_011529317.1:p.Cys110=
NM_006517.5:c.330C>T MANE Select NP_006508.2:p.Cys110=
Search 100 bp 5'
Search 100 bp 3'