Canonical Allele Identifier: CA821943351

Gene:

Linked Data

• dbSNP Id: rs10945919
• MyVariant Identifiers: chr6:g.164186677A>C (hg19) ; chr6:g.163765645A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.163765645A>C , CM000668.2:g.163765645A>C	GRCh38
NC_000006.11:g.164186677A>C , CM000668.1:g.164186677A>C	GRCh37
NC_000006.10:g.164106667A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001744452.1:n.410+6216A>C
XR_001744454.1:n.369+6257A>C
XR_001744455.1:n.346+6280A>C