Canonical Allele Identifier: CA270150967
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs932837377

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251879A>C , CM000677.2:g.45251879A>C GRCh38
NC_000015.9:g.45544077A>C , CM000677.1:g.45544077A>C GRCh37
NC_000015.8:g.43331369A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.374T>G