Canonical Allele Identifier: CA2649031437

Gene: SLC19A2

Linked Data

• gnomAD v4: 1-169485469-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485469T>C , CM000663.2:g.169485469T>C	GRCh38
NC_000001.10:g.169454707T>C , CM000663.1:g.169454707T>C	GRCh37
NC_000001.9:g.167721331T>C	NCBI36
NG_008255.1:g.5502A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.204+94A>G MANE Select	ENSP00000236137.5:n.204+94A>G
ENST00000646596.1:c.204+94A>G	ENSP00000494404.1:n.204+94A>G
ENST00000236137.9:c.204+94A>G	ENSP00000236137.5:n.204+94A>G
ENST00000367804.4:c.204+94A>G	ENSP00000356778.3:n.204+94A>G
NM_006996.2:c.204+94A>G	NP_008927.1:n.204+94A>G
XM_011509076.1:c.12+584A>G	XP_011507378.1:n.12+584A>G
XM_011509077.1:c.204+94A>G	XP_011507379.1:n.204+94A>G
NM_001319667.1:c.204+94A>G	NP_001306596.1:n.204+94A>G
NM_006996.3:c.204+94A>G MANE Select	NP_008927.1:n.204+94A>G