Canonical Allele Identifier: CA829129720

Gene:

Linked Data

• dbSNP Id: rs1332542933
• MyVariant Identifiers: chr6:g.86691971C>G (hg19) ; chr6:g.85982253C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.85982253C>G , CM000668.2:g.85982253C>G	GRCh38
NC_000006.11:g.86691971C>G , CM000668.1:g.86691971C>G	GRCh37
NC_000006.10:g.86748690C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_241869.3:n.615-11127C>G
XR_942747.1:n.41-1116C>G
XR_942748.1:n.27-1116C>G
XR_001744239.1:n.1570-11127C>G
XR_001744243.1:n.1433-11127C>G
XR_002956361.1:n.1992-11127C>G