Canonical Allele Identifier: CA2649031504
Gene: SLC19A2 HGNC NCBI

Linked Data

gnomAD v4: 1-169485525-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169485525C>T , CM000663.2:g.169485525C>T GRCh38
NC_000001.10:g.169454763C>T , CM000663.1:g.169454763C>T GRCh37
NC_000001.9:g.167721387C>T NCBI36
NG_008255.1:g.5446G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000236137.10:c.204+38G>A MANE Select ENSP00000236137.5:n.204+38G>A
ENST00000646596.1:c.204+38G>A ENSP00000494404.1:n.204+38G>A
ENST00000236137.9:c.204+38G>A ENSP00000236137.5:n.204+38G>A
ENST00000367804.4:c.204+38G>A ENSP00000356778.3:n.204+38G>A
NM_006996.2:c.204+38G>A NP_008927.1:n.204+38G>A
XM_011509076.1:c.12+528G>A XP_011507378.1:n.12+528G>A
XM_011509077.1:c.204+38G>A XP_011507379.1:n.204+38G>A
NM_001319667.1:c.204+38G>A NP_001306596.1:n.204+38G>A
NM_006996.3:c.204+38G>A MANE Select NP_008927.1:n.204+38G>A
Search 100 bp 5'
Search 100 bp 3'