Canonical Allele Identifier: CA1601790160

Gene:

Linked Data

• dbSNP Id: rs1765089397

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173507872C>T , CM000667.2:g.173507872C>T	GRCh38
NC_000005.9:g.172934875C>T , CM000667.1:g.172934875C>T	GRCh37
NC_000005.8:g.172867481C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941238.1:n.5641+282C>T
XR_941239.1:n.3602+282C>T
XR_941240.1:n.5497+282C>T
XR_941241.1:n.3078+282C>T
XR_941242.1:n.5391+282C>T
XR_941243.1:n.5568+282C>T
XR_941244.1:n.2883+282C>T
XR_941246.1:n.5261+282C>T
XR_001743000.1:n.3529+282C>T
XR_001743001.1:n.3056+282C>T
XR_002956234.1:n.5200+282C>T