Canonical Allele Identifier: CA244637519

Gene:

Linked Data

• dbSNP Id: rs921233718
• MyVariant Identifiers: chr12:g.115836426G>A (hg19) ; chr12:g.115398621G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115398621G>A , CM000674.2:g.115398621G>A	GRCh38
NC_000012.11:g.115836426G>A , CM000674.1:g.115836426G>A	GRCh37
NC_000012.10:g.114320809G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_945389.1:n.697+8474C>T
XR_945389.2:n.701+8474C>T