Canonical Allele Identifier: CA517464589
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74421928-T-C
MyVariant Identifiers: chrX:g.73641763T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421928T>C , CM000685.2:g.74421928T>C GRCh38
NC_000023.10:g.73641763T>C , CM000685.1:g.73641763T>C GRCh37
NC_000023.9:g.73558488T>C NCBI36
NG_011641.1:g.5679T>C
NG_011641.2:g.5679T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.291T>C MANE Select ENSP00000465734.1:p.Gly97=
ENST00000636771.1:c.37T>C
ENST00000587091.5:c.291T>C ENSP00000465734.1:p.Gly97=
NM_006517.4:c.291T>C NP_006508.2:p.Gly97=
XM_005262294.1:c.291T>C XP_005262351.1:p.Gly97=
XM_011531015.1:c.291T>C XP_011529317.1:p.Gly97=
NM_006517.5:c.291T>C MANE Select NP_006508.2:p.Gly97=
Search 100 bp 5'
Search 100 bp 3'