Canonical Allele Identifier: CA150690537

Gene:

Identifiers and link-outs to other resources

• dbSNP Id: rs10499299
• gnomAD: 6:156133888 A / G
• MyVariant Identifiers: chr6:g.156133888A>G (hg19) ; chr6:g.155812754A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812754A>G , CM000668.2:g.155812754A>G	GRCh38
NC_000006.11:g.156133888A>G , CM000668.1:g.156133888A>G	GRCh37
NC_000006.10:g.156175580A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943142.1:n.79+19335A>G
XR_943146.1:n.645-715T>C
XR_001744423.1:n.699-715T>C
XR_001744424.1:n.79+19335A>G