Canonical Allele Identifier: CA1143696290

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485567C= , CM000663.2:g.169485567C=	GRCh38
NC_000001.10:g.169454805C= , CM000663.1:g.169454805C=	GRCh37
NC_000001.9:g.167721429C=	NCBI36
NG_008255.1:g.5404G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.200G= MANE Select	ENSP00000236137.5:p.Arg67=
ENST00000646596.1:c.200G=	ENSP00000494404.1:p.Arg67=
ENST00000236137.9:c.200G=	ENSP00000236137.5:p.Arg67=
ENST00000367804.4:c.200G=	ENSP00000356778.3:p.Arg67=
NM_006996.2:c.200G=	NP_008927.1:p.Arg67=
XM_011509076.1:c.12+486G=	XP_011507378.1:n.12+486G=
XM_011509077.1:c.200G=	XP_011507379.1:p.Arg67=
NM_001319667.1:c.200G=	NP_001306596.1:p.Arg67=
NM_006996.3:c.200G= MANE Select	NP_008927.1:p.Arg67=