Canonical Allele Identifier: CA275015077

Gene:

Linked Data

• dbSNP Id: rs898800098
• MyVariant Identifiers: chr15:g.87962551C>T (hg19) ; chr15:g.87419320C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87419320C>T , CM000677.2:g.87419320C>T	GRCh38
NC_000015.9:g.87962551C>T , CM000677.1:g.87962551C>T	GRCh37
NC_000015.8:g.85763555C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_932584.1:n.340-49G>A
XR_932585.1:n.340-49G>A
XR_001751647.1:n.617-49G>A
XR_932585.2:n.627-49G>A