Canonical Allele Identifier: CA413655848
Gene: SLC16A2 HGNC NCBI

Linked Data

dbSNP Id: rs1199581637

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74421771C>T , CM000685.2:g.74421771C>T GRCh38
NC_000023.10:g.73641606C>T , CM000685.1:g.73641606C>T GRCh37
NC_000023.9:g.73558331C>T NCBI36
NG_011641.1:g.5522C>T
NG_011641.2:g.5522C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.134C>T MANE Select ENSP00000465734.1:p.Pro45Leu
ENST00000587091.5:c.134C>T ENSP00000465734.1:p.Pro45Leu
NM_006517.4:c.134C>T NP_006508.2:p.Pro45Leu
XM_005262294.1:c.134C>T XP_005262351.1:p.Pro45Leu
XM_011531015.1:c.134C>T XP_011529317.1:p.Pro45Leu
NM_006517.5:c.134C>T MANE Select NP_006508.2:p.Pro45Leu