Canonical Allele Identifier: CA15422753

Gene:

Linked Data

• dbSNP Id: rs10945919
• gnomAD v2: 6-164186677-A-G
• gnomAD v3: 6-163765645-A-G
• gnomAD v4: 6-163765645-A-G
• MyVariant Identifiers: chr6:g.164186677A>G (hg19) ; chr6:g.163765645A>G (hg38)

Genomic Alleles

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

Transcript Alleles

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