Canonical Allele Identifier: CA460228696
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034280T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176764T>A , CM000670.2:g.31176764T>A GRCh38
NC_000008.10:g.31034280T>A , CM000670.1:g.31034280T>A GRCh37
NC_000008.9:g.31153822T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.293T>A
XR_949643.1:n.15A>T
XR_949644.1:n.15A>T
XR_949645.1:n.15A>T
XR_949646.1:n.15A>T
XR_949647.1:n.628A>T
XR_949648.1:n.530A>T