Canonical Allele Identifier: CA649191427

Gene:

Linked Data

• dbSNP Id: rs1224524028
• COSMIC: COSN20156769
• MyVariant Identifiers: chr4:g.135522747T>C (hg19) ; chr4:g.134601592T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.134601592T>C , CM000666.2:g.134601592T>C	GRCh38
NC_000004.11:g.135522747T>C , CM000666.1:g.135522747T>C	GRCh37
NC_000004.10:g.135742197T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_939212.1:n.410+14233T>C
XR_939214.1:n.392+14233T>C
XR_939214.2:n.392+14233T>C