Canonical Allele Identifier: CA756174712

Gene:

Linked Data

• dbSNP Id: rs12711580
• MyVariant Identifiers: chr2:g.123126868T>A (hg19) ; chr2:g.122369292T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122369292T>A , CM000664.2:g.122369292T>A	GRCh38
NC_000002.11:g.123126868T>A , CM000664.1:g.123126868T>A	GRCh37
NC_000002.10:g.122843338T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-23671T>A
XR_001739684.1:n.556-23671T>A