Canonical Allele Identifier: CA460228685
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034276G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176760G>C , CM000670.2:g.31176760G>C GRCh38
NC_000008.10:g.31034276G>C , CM000670.1:g.31034276G>C GRCh37
NC_000008.9:g.31153818G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.289G>C
XR_949643.1:n.19C>G
XR_949644.1:n.19C>G
XR_949645.1:n.19C>G
XR_949646.1:n.19C>G
XR_949647.1:n.632C>G
XR_949648.1:n.534C>G