Canonical Allele Identifier: CA1595159542

Gene:

Linked Data

• dbSNP Id: rs1160128752

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159581012C>T , CM000667.2:g.159581012C>T	GRCh38
NC_000005.9:g.159008019C>T , CM000667.1:g.159008019C>T	GRCh37
NC_000005.8:g.158940597C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941139.1:n.2075+577C>T
XR_941140.1:n.2075+577C>T
XR_941141.1:n.570+577C>T
XR_941139.2:n.2229+577C>T