Canonical Allele Identifier: CA1206116058

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485332C= , CM000663.2:g.169485332C=	GRCh38
NC_000001.10:g.169454570C= , CM000663.1:g.169454570C=	GRCh37
NC_000001.9:g.167721194C=	NCBI36
NG_008255.1:g.5639G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.204+231G= MANE Select	ENSP00000236137.5:n.204+231G=
ENST00000646596.1:c.204+231G=	ENSP00000494404.1:n.204+231G=
ENST00000236137.9:c.204+231G=	ENSP00000236137.5:n.204+231G=
ENST00000367804.4:c.204+231G=	ENSP00000356778.3:n.204+231G=
NM_006996.2:c.204+231G=	NP_008927.1:n.204+231G=
XM_011509076.1:c.12+721G=	XP_011507378.1:n.12+721G=
XM_011509077.1:c.204+231G=	XP_011507379.1:n.204+231G=
NM_001319667.1:c.204+231G=	NP_001306596.1:n.204+231G=
NM_006996.3:c.204+231G= MANE Select	NP_008927.1:n.204+231G=