Canonical Allele Identifier: CA2628262758
Gene: SLC28A2 HGNC NCBI
SLC28A2-AS1 HGNC NCBI

Linked Data

gnomAD v4: 15-45262111-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45262111G>T , CM000677.2:g.45262111G>T GRCh38
NC_000015.9:g.45554309G>T , CM000677.1:g.45554309G>T GRCh37
NC_000015.8:g.43341601G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347644.8:c.262+5G>T (SLC28A2) MANE Select ENSP00000315006.4:n.262+5G>T
ENST00000347644.7:c.262+5G>T (SLC28A2) ENSP00000315006.4:n.262+5G>T
ENST00000560438.5:c.226+5G>T (SLC28A2) ENSP00000454074.1:n.226+5G>T
NM_004212.3:c.262+5G>T (SLC28A2) NP_004203.2:n.262+5G>T
NR_120335.1:n.27-6113C>A (SLC28A2-AS1)
XM_011522198.1:c.262+5G>T (SLC28A2) XP_011520500.1:n.262+5G>T
XM_011522199.1:c.262+5G>T (SLC28A2) XP_011520501.1:n.262+5G>T
XM_011522200.1:c.262+5G>T (SLC28A2) XP_011520502.1:n.262+5G>T
XM_011522201.1:c.262+5G>T (SLC28A2) XP_011520503.1:n.262+5G>T
XM_011522198.2:c.262+5G>T (SLC28A2) XP_011520500.1:n.262+5G>T
XM_011522200.2:c.262+5G>T (SLC28A2) XP_011520502.1:n.262+5G>T
XM_011522201.2:c.262+5G>T (SLC28A2) XP_011520503.1:n.262+5G>T
NM_004212.4:c.262+5G>T (SLC28A2) MANE Select NP_004203.2:n.262+5G>T
Search 100 bp 5'
Search 100 bp 3'