Canonical Allele Identifier: CA1206116182

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485497T= , CM000663.2:g.169485497T=	GRCh38
NC_000001.10:g.169454735T= , CM000663.1:g.169454735T=	GRCh37
NC_000001.9:g.167721359T=	NCBI36
NG_008255.1:g.5474A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.204+66A= MANE Select	ENSP00000236137.5:n.204+66A=
ENST00000646596.1:c.204+66A=	ENSP00000494404.1:n.204+66A=
ENST00000236137.9:c.204+66A=	ENSP00000236137.5:n.204+66A=
ENST00000367804.4:c.204+66A=	ENSP00000356778.3:n.204+66A=
NM_006996.2:c.204+66A=	NP_008927.1:n.204+66A=
XM_011509076.1:c.12+556A=	XP_011507378.1:n.12+556A=
XM_011509077.1:c.204+66A=	XP_011507379.1:n.204+66A=
NM_001319667.1:c.204+66A=	NP_001306596.1:n.204+66A=
NM_006996.3:c.204+66A= MANE Select	NP_008927.1:n.204+66A=