Canonical Allele Identifier: CA692802661

Gene:

Linked Data

• dbSNP Id: rs1220212291
• gnomAD v3: 12-84952164-T-C
• gnomAD v4: 12-84952164-T-C
• MyVariant Identifiers: chr12:g.85345943T>C (hg19) ; chr12:g.84952164T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.84952164T>C , CM000674.2:g.84952164T>C	GRCh38
NC_000012.11:g.85345943T>C , CM000674.1:g.85345943T>C	GRCh37
NC_000012.10:g.83870074T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945152.1:n.316+30850T>C
XR_945153.1:n.301+13700T>C
XR_945154.1:n.175-36778T>C
XR_945155.1:n.330+30850T>C
XR_945152.2:n.316+30850T>C
XR_945154.2:n.175-36778T>C
XR_945155.2:n.888+30850T>C