Canonical Allele Identifier: CA1206116187

Gene: SLC19A2

Linked Data

• dbSNP Id: rs1658535627
• gnomAD v4: 1-169485501-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485501T>A , CM000663.2:g.169485501T>A	GRCh38
NC_000001.10:g.169454739T>A , CM000663.1:g.169454739T>A	GRCh37
NC_000001.9:g.167721363T>A	NCBI36
NG_008255.1:g.5470A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.204+62A>T MANE Select	ENSP00000236137.5:n.204+62A>T
ENST00000646596.1:c.204+62A>T	ENSP00000494404.1:n.204+62A>T
ENST00000236137.9:c.204+62A>T	ENSP00000236137.5:n.204+62A>T
ENST00000367804.4:c.204+62A>T	ENSP00000356778.3:n.204+62A>T
NM_006996.2:c.204+62A>T	NP_008927.1:n.204+62A>T
XM_011509076.1:c.12+552A>T	XP_011507378.1:n.12+552A>T
XM_011509077.1:c.204+62A>T	XP_011507379.1:n.204+62A>T
NM_001319667.1:c.204+62A>T	NP_001306596.1:n.204+62A>T
NM_006996.3:c.204+62A>T MANE Select	NP_008927.1:n.204+62A>T