Canonical Allele Identifier: CA460228692
Gene:

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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