Canonical Allele Identifier: CA273056094

Gene:

Linked Data

• dbSNP Id: rs910487725
• MyVariant Identifiers: chr15:g.69755662T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.69755662T>A , CM000677.2:g.69755662T>A	GRCh38
NC_000015.9:g.70048001T>A , CM000677.1:g.70048001T>A	GRCh37
NC_000015.8:g.67835055T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751592.2:n.86-494T>A