Canonical Allele Identifier: CA820839151

Gene:

Linked Data

• dbSNP Id: rs1470023007
• MyVariant Identifiers: chr6:g.151954648A>G (hg19) ; chr6:g.151633513A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633513A>G , CM000668.2:g.151633513A>G	GRCh38
NC_000006.11:g.151954648A>G , CM000668.1:g.151954648A>G	GRCh37
NC_000006.10:g.151996341A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3531A>G