Canonical Allele Identifier: CA1206117440

Gene: SLC19A2

Linked Data

• dbSNP Id: rs1658551595

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485791_169485794del , CM000663.2:g.169485791_169485794del	GRCh38
NC_000001.10:g.169455029_169455032del , CM000663.1:g.169455029_169455032del	GRCh37
NC_000001.9:g.167721653_167721656del	NCBI36
NG_008255.1:g.5179_5182del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.-26_-23del MANE Select	ENSP00000236137.5:n.-26_-23del
ENST00000646596.1:c.-26_-23del	ENSP00000494404.1:n.-26_-23del
ENST00000236137.9:c.-26_-23del	ENSP00000236137.5:n.-26_-23del
ENST00000367804.4:c.-26_-23del	ENSP00000356778.3:n.-26_-23del
NM_006996.2:c.-26_-23del	NP_008927.1:n.-26_-23del
XM_011509076.1:c.12+261_12+264del	XP_011507378.1:n.12+261_12+264del
XM_011509077.1:c.-26_-23del	XP_011507379.1:n.-26_-23del
NM_001319667.1:c.-26_-23del	NP_001306596.1:n.-26_-23del
NM_006996.3:c.-26_-23del MANE Select	NP_008927.1:n.-26_-23del