Canonical Allele Identifier: CA133613607

Gene:

Linked Data

• dbSNP Id: rs967039373
• gnomAD v3: 6-1535876-A-G
• gnomAD v4: 6-1535876-A-G
• MyVariant Identifiers: chr6:g.1536111A>G (hg19) ; chr6:g.1535876A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1535876A>G , CM000668.2:g.1535876A>G	GRCh38
NC_000006.11:g.1536111A>G , CM000668.1:g.1536111A>G	GRCh37
NC_000006.10:g.1481110A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_427861.2:n.234+16470T>C
XR_926380.1:n.218-2580A>G
XR_926381.1:n.1108-2580A>G
XR_926382.1:n.235-6697T>C
XR_926384.1:n.200-6697T>C
XR_001743921.1:n.235-6721T>C
XR_427861.3:n.234+16470T>C
XR_926381.2:n.1123-2580A>G