Canonical Allele Identifier: CA46769580

Gene:

Linked Data

• dbSNP Id: rs902580552
• MyVariant Identifiers: chr2:g.41534677G>C (hg38)

Genomic Alleles

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

Transcript Alleles

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