Canonical Allele Identifier: CA12286197

Gene:

Linked Data

• dbSNP Id: rs10946292
• gnomAD v2: 6-170425521-A-G
• gnomAD v3: 6-170110297-A-G
• gnomAD v4: 6-170110297-A-G
• MyVariant Identifiers: chr6:g.170425521A>G (hg19) ; chr6:g.170110297A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.170110297A>G , CM000668.2:g.170110297A>G	GRCh38
NC_000006.11:g.170425521A>G , CM000668.1:g.170425521A>G	GRCh37
NC_000006.10:g.170267446A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943319.1:n.566-2837T>C
XR_943320.1:n.566-2837T>C