Canonical Allele Identifier: CA692802611

Gene:

Linked Data

• dbSNP Id: rs1426900222
• gnomAD v3: 12-84952113-A-C
• gnomAD v4: 12-84952113-A-C
• MyVariant Identifiers: chr12:g.85345892A>C (hg19) ; chr12:g.84952113A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.84952113A>C , CM000674.2:g.84952113A>C	GRCh38
NC_000012.11:g.85345892A>C , CM000674.1:g.85345892A>C	GRCh37
NC_000012.10:g.83870023A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945152.1:n.316+30799A>C
XR_945153.1:n.301+13649A>C
XR_945154.1:n.175-36829A>C
XR_945155.1:n.330+30799A>C
XR_945152.2:n.316+30799A>C
XR_945154.2:n.175-36829A>C
XR_945155.2:n.888+30799A>C