Canonical Allele Identifier: CA460228707
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034283T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176767T>C , CM000670.2:g.31176767T>C GRCh38
NC_000008.10:g.31034283T>C , CM000670.1:g.31034283T>C GRCh37
NC_000008.9:g.31153825T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.296T>C
XR_949643.1:n.12A>G
XR_949644.1:n.12A>G
XR_949645.1:n.12A>G
XR_949646.1:n.12A>G
XR_949647.1:n.625A>G
XR_949648.1:n.527A>G