Canonical Allele Identifier: CA1595159573
Gene:

Linked Data

dbSNP Id: rs1562184966

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159581047C>G , CM000667.2:g.159581047C>G GRCh38
NC_000005.9:g.159008054C>G , CM000667.1:g.159008054C>G GRCh37
NC_000005.8:g.158940632C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+612C>G
XR_941140.1:n.2075+612C>G
XR_941141.1:n.570+612C>G
XR_941139.2:n.2229+612C>G