Canonical Allele Identifier: CA1142491095

Gene: SLC19A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485789C= , CM000663.2:g.169485789C=	GRCh38
NC_000001.10:g.169455027C= , CM000663.1:g.169455027C=	GRCh37
NC_000001.9:g.167721651C=	NCBI36
NG_008255.1:g.5182G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.-23G= MANE Select	ENSP00000236137.5:n.-23G=
ENST00000646596.1:c.-23G=	ENSP00000494404.1:n.-23G=
ENST00000236137.9:c.-23G=	ENSP00000236137.5:n.-23G=
ENST00000367804.4:c.-23G=	ENSP00000356778.3:n.-23G=
NM_006996.2:c.-23G=	NP_008927.1:n.-23G=
XM_011509076.1:c.12+264G=	XP_011507378.1:n.12+264G=
XM_011509077.1:c.-23G=	XP_011507379.1:n.-23G=
NM_001319667.1:c.-23G=	NP_001306596.1:n.-23G=
NM_006996.3:c.-23G= MANE Select	NP_008927.1:n.-23G=