Canonical Allele Identifier: CA150162895

Gene:

Linked Data

• dbSNP Id: rs1028594890
• MyVariant Identifiers: chr6:g.151954708A>T (hg19) ; chr6:g.151633573A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633573A>T , CM000668.2:g.151633573A>T	GRCh38
NC_000006.11:g.151954708A>T , CM000668.1:g.151954708A>T	GRCh37
NC_000006.10:g.151996401A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3591A>T