Canonical Allele Identifier: CA392251473

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• dbSNP Id: rs11854484
• gnomAD v3: 15-45253280-C-G
• gnomAD v4: 15-45253280-C-G
• MyVariant Identifiers: chr15:g.45545478C>G (hg19) ; chr15:g.45253280C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45253280C>G , CM000677.2:g.45253280C>G	GRCh38
NC_000015.9:g.45545478C>G , CM000677.1:g.45545478C>G	GRCh37
NC_000015.8:g.43332770C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000347644.8:c.65C>G (SLC28A2) MANE Select	ENSP00000315006.4:p.Pro22Arg
ENST00000347644.7:c.65C>G (SLC28A2)	ENSP00000315006.4:p.Pro22Arg
ENST00000560438.5:c.46-152C>G (SLC28A2)	ENSP00000454074.1:n.46-152C>G
NM_004212.3:c.65C>G (SLC28A2)	NP_004203.2:p.Pro22Arg
NR_120335.1:n.180+586G>C (SLC28A2-AS1)
XM_011522198.1:c.65C>G (SLC28A2)	XP_011520500.1:p.Pro22Arg
XM_011522199.1:c.65C>G (SLC28A2)	XP_011520501.1:p.Pro22Arg
XM_011522200.1:c.65C>G (SLC28A2)	XP_011520502.1:p.Pro22Arg
XM_011522201.1:c.65C>G (SLC28A2)	XP_011520503.1:p.Pro22Arg
XM_011522198.2:c.65C>G (SLC28A2)	XP_011520500.1:p.Pro22Arg
XM_011522200.2:c.65C>G (SLC28A2)	XP_011520502.1:p.Pro22Arg
XM_011522201.2:c.65C>G (SLC28A2)	XP_011520503.1:p.Pro22Arg
NM_004212.4:c.65C>G (SLC28A2) MANE Select	NP_004203.2:p.Pro22Arg