Canonical Allele Identifier: CA476840361

Gene:

Linked Data

• dbSNP Id: rs1591854006
• MyVariant Identifiers: chr11:g.114231372A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.114360650A>G , CM000673.2:g.114360650A>G	GRCh38
NC_000011.9:g.114231372A>G , CM000673.1:g.114231372A>G	GRCh37
NC_000011.8:g.113736582A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120567.1:n.3816T>C