Canonical Allele Identifier: CA1595159091
Gene:

Linked Data

dbSNP Id: rs1757450940

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580755T>C , CM000667.2:g.159580755T>C GRCh38
NC_000005.9:g.159007763T>C , CM000667.1:g.159007763T>C GRCh37
NC_000005.8:g.158940341T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+320T>C
XR_941140.1:n.2075+320T>C
XR_941141.1:n.570+320T>C
XR_941139.2:n.2229+320T>C