Canonical Allele Identifier: CA421719892

Gene: SLC19A2

Linked Data

• MyVariant Identifiers: chr1:g.169454984C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485746C>T , CM000663.2:g.169485746C>T	GRCh38
NC_000001.10:g.169454984C>T , CM000663.1:g.169454984C>T	GRCh37
NC_000001.9:g.167721608C>T	NCBI36
NG_008255.1:g.5225G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.21G>A MANE Select	ENSP00000236137.5:p.Val7=
ENST00000646596.1:c.21G>A	ENSP00000494404.1:p.Val7=
ENST00000236137.9:c.21G>A	ENSP00000236137.5:p.Val7=
ENST00000367804.4:c.21G>A	ENSP00000356778.3:p.Val7=
NM_006996.2:c.21G>A	NP_008927.1:p.Val7=
XM_011509076.1:c.12+307G>A	XP_011507378.1:n.12+307G>A
XM_011509077.1:c.21G>A	XP_011507379.1:p.Val7=
NM_001319667.1:c.21G>A	NP_001306596.1:p.Val7=
NM_006996.3:c.21G>A MANE Select	NP_008927.1:p.Val7=