Canonical Allele Identifier: CA460228515
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034216C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176700C>T , CM000670.2:g.31176700C>T GRCh38
NC_000008.10:g.31034216C>T , CM000670.1:g.31034216C>T GRCh37
NC_000008.9:g.31153758C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.271-42C>T
XR_949643.1:n.79G>A
XR_949644.1:n.79G>A
XR_949645.1:n.79G>A
XR_949646.1:n.79G>A
XR_949647.1:n.692G>A
XR_949648.1:n.594G>A