Canonical Allele Identifier: CA1595159028
Gene:

Linked Data

dbSNP Id: rs1757450380

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580683T>C , CM000667.2:g.159580683T>C GRCh38
NC_000005.9:g.159007691T>C , CM000667.1:g.159007691T>C GRCh37
NC_000005.8:g.158940269T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+248T>C
XR_941140.1:n.2075+248T>C
XR_941141.1:n.570+248T>C
XR_941139.2:n.2229+248T>C