Canonical Allele Identifier: CA460228694
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034279G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176763G>C , CM000670.2:g.31176763G>C GRCh38
NC_000008.10:g.31034279G>C , CM000670.1:g.31034279G>C GRCh37
NC_000008.9:g.31153821G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.292G>C
XR_949643.1:n.16C>G
XR_949644.1:n.16C>G
XR_949645.1:n.16C>G
XR_949646.1:n.16C>G
XR_949647.1:n.629C>G
XR_949648.1:n.531C>G