Canonical Allele Identifier: CA460228726
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034290A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176774A>C , CM000670.2:g.31176774A>C GRCh38
NC_000008.10:g.31034290A>C , CM000670.1:g.31034290A>C GRCh37
NC_000008.9:g.31153832A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.303A>C
XR_949643.1:n.5T>G
XR_949644.1:n.5T>G
XR_949645.1:n.5T>G
XR_949646.1:n.5T>G
XR_949647.1:n.618T>G
XR_949648.1:n.520T>G