Canonical Allele Identifier: CA1595159322
Gene:

Linked Data

dbSNP Id: rs1757452247

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580889A>C , CM000667.2:g.159580889A>C GRCh38
NC_000005.9:g.159007897A>C , CM000667.1:g.159007897A>C GRCh37
NC_000005.8:g.158940475A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+454A>C
XR_941140.1:n.2075+454A>C
XR_941141.1:n.570+454A>C
XR_941139.2:n.2229+454A>C