Canonical Allele Identifier: CA460228691
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034278T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176762T>G , CM000670.2:g.31176762T>G GRCh38
NC_000008.10:g.31034278T>G , CM000670.1:g.31034278T>G GRCh37
NC_000008.9:g.31153820T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.291T>G
XR_949643.1:n.17A>C
XR_949644.1:n.17A>C
XR_949645.1:n.17A>C
XR_949646.1:n.17A>C
XR_949647.1:n.630A>C
XR_949648.1:n.532A>C