Canonical Allele Identifier: CA12221539
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs11242704

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535763A>G , CM000668.2:g.1535763A>G GRCh38
NC_000006.11:g.1535998A>G , CM000668.1:g.1535998A>G GRCh37
NC_000006.10:g.1480997A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427861.2:n.234+16583T>C
XR_926380.1:n.218-2693A>G
XR_926381.1:n.1108-2693A>G
XR_926382.1:n.235-6584T>C
XR_926384.1:n.200-6584T>C
XR_001743921.1:n.235-6608T>C
XR_427861.3:n.234+16583T>C
XR_926381.2:n.1123-2693A>G