Canonical Allele Identifier: CA820836185

Gene:

Linked Data

• dbSNP Id: rs1412224472
• MyVariant Identifiers: chr6:g.151948285A>T (hg19) ; chr6:g.151627150A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151627150A>T , CM000668.2:g.151627150A>T	GRCh38
NC_000006.11:g.151948285A>T , CM000668.1:g.151948285A>T	GRCh37
NC_000006.10:g.151989978A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943113.1:n.576A>T
XR_943115.1:n.576A>T