Canonical Allele Identifier: CA460228507
Gene:

Linked Data

MyVariant Identifiers: chr8:g.31034214C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176698C>A , CM000670.2:g.31176698C>A GRCh38
NC_000008.10:g.31034214C>A , CM000670.1:g.31034214C>A GRCh37
NC_000008.9:g.31153756C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.271-44C>A
XR_949643.1:n.81G>T
XR_949644.1:n.81G>T
XR_949645.1:n.81G>T
XR_949646.1:n.81G>T
XR_949647.1:n.694G>T
XR_949648.1:n.596G>T