Canonical Allele Identifier: CA2437472617
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421862C= , CM000685.2:g.74421862C= GRCh38
NC_000023.10:g.73641697C= , CM000685.1:g.73641697C= GRCh37
NC_000023.9:g.73558422C= NCBI36
NG_011641.1:g.5613C=
NG_011641.2:g.5613C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.225C= MANE Select ENSP00000465734.1:p.His75=
ENST00000587091.5:c.225C= ENSP00000465734.1:p.His75=
NM_006517.4:c.225C= NP_006508.2:p.His75=
XM_005262294.1:c.225C= XP_005262351.1:p.His75=
XM_011531015.1:c.225C= XP_011529317.1:p.His75=
NM_006517.5:c.225C= MANE Select NP_006508.2:p.His75=