Canonical Allele Identifier: CA618007798

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• dbSNP Id: rs746721673
• gnomAD v2: 15-45559795-T-A
• gnomAD v3: 15-45267597-T-A
• gnomAD v4: 15-45267597-T-A
• MyVariant Identifiers: chr15:g.45559795T>A (hg19) ; chr15:g.45267597T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45267597T>A , CM000677.2:g.45267597T>A	GRCh38
NC_000015.9:g.45559795T>A , CM000677.1:g.45559795T>A	GRCh37
NC_000015.8:g.43347087T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000347644.8:c.1068+17T>A (SLC28A2) MANE Select	ENSP00000315006.4:n.1068+17T>A
ENST00000347644.7:c.1068+17T>A (SLC28A2)	ENSP00000315006.4:n.1068+17T>A
ENST00000559924.1:c.682+17T>A (SLC28A2)
NM_004212.3:c.1068+17T>A (SLC28A2)	NP_004203.2:n.1068+17T>A
NR_120335.1:n.27-11599A>T (SLC28A2-AS1)
XM_011522198.1:c.1068+17T>A (SLC28A2)	XP_011520500.1:n.1068+17T>A
XM_011522199.1:c.1068+17T>A (SLC28A2)	XP_011520501.1:n.1068+17T>A
XM_011522200.1:c.1068+17T>A (SLC28A2)	XP_011520502.1:n.1068+17T>A
XM_011522201.1:c.1068+17T>A (SLC28A2)	XP_011520503.1:n.1068+17T>A
XM_011522202.1:c.183+17T>A (SLC28A2)	XP_011520504.1:n.183+17T>A
XM_011522198.2:c.1068+17T>A (SLC28A2)	XP_011520500.1:n.1068+17T>A
XM_011522200.2:c.1068+17T>A (SLC28A2)	XP_011520502.1:n.1068+17T>A
XM_011522201.2:c.1068+17T>A (SLC28A2)	XP_011520503.1:n.1068+17T>A
XM_011522202.2:c.183+17T>A (SLC28A2)	XP_011520504.1:n.183+17T>A
NM_004212.4:c.1068+17T>A (SLC28A2) MANE Select	NP_004203.2:n.1068+17T>A