Canonical Allele Identifier: CA150163048

Gene:

Linked Data

• dbSNP Id: rs918235251
• MyVariant Identifiers: chr6:g.151954891C>T (hg19) ; chr6:g.151633756C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633756C>T , CM000668.2:g.151633756C>T	GRCh38
NC_000006.11:g.151954891C>T , CM000668.1:g.151954891C>T	GRCh37
NC_000006.10:g.151996584C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943115.1:n.2496+3774C>T