Canonical Allele Identifier: CA768889964

Gene:

Linked Data

• dbSNP Id: rs902580552
• MyVariant Identifiers: chr2:g.41761817G>A (hg19) ; chr2:g.41534677G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.41534677G>A , CM000664.2:g.41534677G>A	GRCh38
NC_000002.11:g.41761817G>A , CM000664.1:g.41761817G>A	GRCh37
NC_000002.10:g.41615321G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_939996.1:n.181+3049C>T
XR_939997.1:n.146+3049C>T
XR_939997.2:n.9529+3049C>T