Canonical Allele Identifier: CA343112087
Gene: SLC19A2 HGNC NCBI

Linked Data

dbSNP Id: rs1224877258

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169485573G>A , CM000663.2:g.169485573G>A GRCh38
NC_000001.10:g.169454811G>A , CM000663.1:g.169454811G>A GRCh37
NC_000001.9:g.167721435G>A NCBI36
NG_008255.1:g.5398C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000236137.10:c.194C>T MANE Select ENSP00000236137.5:p.Thr65Ile
ENST00000646596.1:c.194C>T ENSP00000494404.1:p.Thr65Ile
ENST00000236137.9:c.194C>T ENSP00000236137.5:p.Thr65Ile
ENST00000367804.4:c.194C>T ENSP00000356778.3:p.Thr65Ile
NM_006996.2:c.194C>T NP_008927.1:p.Thr65Ile
XM_011509076.1:c.12+480C>T XP_011507378.1:n.12+480C>T
XM_011509077.1:c.194C>T XP_011507379.1:p.Thr65Ile
NM_001319667.1:c.194C>T NP_001306596.1:p.Thr65Ile
NM_006996.3:c.194C>T MANE Select NP_008927.1:p.Thr65Ile