Canonical Allele Identifier: CA1206117329
Gene: SLC19A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169485617C= , CM000663.2:g.169485617C= GRCh38
NC_000001.10:g.169454855C= , CM000663.1:g.169454855C= GRCh37
NC_000001.9:g.167721479C= NCBI36
NG_008255.1:g.5354G=

Transcript Alleles

HGVS Amino-acid change
ENST00000236137.10:c.150G= MANE Select ENSP00000236137.5:p.Glu50=
ENST00000646596.1:c.150G= ENSP00000494404.1:p.Glu50=
ENST00000236137.9:c.150G= ENSP00000236137.5:p.Glu50=
ENST00000367804.4:c.150G= ENSP00000356778.3:p.Glu50=
NM_006996.2:c.150G= NP_008927.1:p.Glu50=
XM_011509076.1:c.12+436G= XP_011507378.1:n.12+436G=
XM_011509077.1:c.150G= XP_011507379.1:p.Glu50=
NM_001319667.1:c.150G= NP_001306596.1:p.Glu50=
NM_006996.3:c.150G= MANE Select NP_008927.1:p.Glu50=