Canonical Allele Identifier: CA460228721
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034288G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176772G>C , CM000670.2:g.31176772G>C GRCh38
NC_000008.10:g.31034288G>C , CM000670.1:g.31034288G>C GRCh37
NC_000008.9:g.31153830G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.301G>C
XR_949643.1:n.7C>G
XR_949644.1:n.7C>G
XR_949645.1:n.7C>G
XR_949646.1:n.7C>G
XR_949647.1:n.620C>G
XR_949648.1:n.522C>G