Canonical Allele Identifier: CA413656143
Gene: SLC16A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73641750A>C (hg19) chrX:g.74421915A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421915A>C , CM000685.2:g.74421915A>C GRCh38
NC_000023.10:g.73641750A>C , CM000685.1:g.73641750A>C GRCh37
NC_000023.9:g.73558475A>C NCBI36
NG_011641.1:g.5666A>C
NG_011641.2:g.5666A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.278A>C MANE Select ENSP00000465734.1:p.Gln93Pro
ENST00000636771.1:c.24A>C
ENST00000587091.5:c.278A>C ENSP00000465734.1:p.Gln93Pro
NM_006517.4:c.278A>C NP_006508.2:p.Gln93Pro
XM_005262294.1:c.278A>C XP_005262351.1:p.Gln93Pro
XM_011531015.1:c.278A>C XP_011529317.1:p.Gln93Pro
NM_006517.5:c.278A>C MANE Select NP_006508.2:p.Gln93Pro
Search 100 bp 5'
Search 100 bp 3'