Canonical Allele Identifier: CA145357694

Gene:

Linked Data

• dbSNP Id: rs10782174
• gnomAD v2: 6-113134476-G-A
• gnomAD v3: 6-112813274-G-A
• gnomAD v4: 6-112813274-G-A
• MyVariant Identifiers: chr6:g.113134476G>A (hg19) ; chr6:g.112813274G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112813274G>A , CM000668.2:g.112813274G>A	GRCh38
NC_000006.11:g.113134476G>A , CM000668.1:g.113134476G>A	GRCh37
NC_000006.10:g.113241169G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001744300.1:n.59+33488C>T
XR_001744301.1:n.63+33488C>T
XR_001744302.1:n.59+33488C>T
XR_001744303.1:n.59+33488C>T