Canonical Allele Identifier: CA43254745
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs1346751

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458298C>T , CM000664.2:g.16458298C>T GRCh38
NC_000002.10:g.16503047C>T NCBI36
NC_000002.11:g.16639566C>T , CM000664.1:g.16639566C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3204G>A