Canonical Allele Identifier: CA460228682
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034275C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176759C>G , CM000670.2:g.31176759C>G GRCh38
NC_000008.10:g.31034275C>G , CM000670.1:g.31034275C>G GRCh37
NC_000008.9:g.31153817C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.288C>G
XR_949643.1:n.20G>C
XR_949644.1:n.20G>C
XR_949645.1:n.20G>C
XR_949646.1:n.20G>C
XR_949647.1:n.633G>C
XR_949648.1:n.535G>C