Canonical Allele Identifier: CA1206116131
Gene: SLC19A2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169485421G= , CM000663.2:g.169485421G= GRCh38
NC_000001.10:g.169454659G= , CM000663.1:g.169454659G= GRCh37
NC_000001.9:g.167721283G= NCBI36
NG_008255.1:g.5550C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000236137.10:c.204+142C= MANE Select ENSP00000236137.5:n.204+142C=
ENST00000646596.1:c.204+142C= ENSP00000494404.1:n.204+142C=
ENST00000236137.9:c.204+142C= ENSP00000236137.5:n.204+142C=
ENST00000367804.4:c.204+142C= ENSP00000356778.3:n.204+142C=
NM_006996.2:c.204+142C= NP_008927.1:n.204+142C=
XM_011509076.1:c.12+632C= XP_011507378.1:n.12+632C=
XM_011509077.1:c.204+142C= XP_011507379.1:n.204+142C=
NM_001319667.1:c.204+142C= NP_001306596.1:n.204+142C=
NM_006996.3:c.204+142C= MANE Select NP_008927.1:n.204+142C=
Search 100 bp 5'
Search 100 bp 3'