Canonical Allele Identifier: CA850756867

Gene:

Linked Data

• dbSNP Id: rs1211578943
• MyVariant Identifiers: chr8:g.31034184G>A (hg19) ; chr8:g.31176668G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31176668G>A , CM000670.2:g.31176668G>A	GRCh38
NC_000008.10:g.31034184G>A , CM000670.1:g.31034184G>A	GRCh37
NC_000008.9:g.31153726G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949642.1:n.271-74G>A
XR_949643.1:n.87+24C>T
XR_949644.1:n.87+24C>T
XR_949645.1:n.87+24C>T
XR_949646.1:n.87+24C>T
XR_949647.1:n.700+24C>T
XR_949648.1:n.602+24C>T