Canonical Allele Identifier: CA460228622

Gene:

Linked Data

• dbSNP Id: rs1804277476
• MyVariant Identifiers: chr8:g.31034254T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31176738T>C , CM000670.2:g.31176738T>C	GRCh38
NC_000008.10:g.31034254T>C , CM000670.1:g.31034254T>C	GRCh37
NC_000008.9:g.31153796T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949642.1:n.271-4T>C
XR_949643.1:n.41A>G
XR_949644.1:n.41A>G
XR_949645.1:n.41A>G
XR_949646.1:n.41A>G
XR_949647.1:n.654A>G
XR_949648.1:n.556A>G