Canonical Allele Identifier: CA150159442

Gene:

Linked Data

• dbSNP Id: rs934672920
• MyVariant Identifiers: chr6:g.151948378A>G (hg19) ; chr6:g.151627243A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151627243A>G , CM000668.2:g.151627243A>G	GRCh38
NC_000006.11:g.151948378A>G , CM000668.1:g.151948378A>G	GRCh37
NC_000006.10:g.151990071A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943113.1:n.669A>G
XR_943115.1:n.669A>G