Canonical Allele Identifier: CA820925282

Gene:

Linked Data

• dbSNP Id: rs1220740959
• MyVariant Identifiers: chr6:g.1535890C>A (hg19) ; chr6:g.1535655C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1535655C>A , CM000668.2:g.1535655C>A	GRCh38
NC_000006.11:g.1535890C>A , CM000668.1:g.1535890C>A	GRCh37
NC_000006.10:g.1480889C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_427861.2:n.234+16691G>T
XR_926380.1:n.218-2801C>A
XR_926381.1:n.1108-2801C>A
XR_926382.1:n.235-6476G>T
XR_926384.1:n.200-6476G>T
XR_001743921.1:n.235-6500G>T
XR_427861.3:n.234+16691G>T
XR_926381.2:n.1123-2801C>A