Canonical Allele Identifier: CA278115118

Gene:

Linked Data

• dbSNP Id: rs1023896930
• MyVariant Identifiers: chr16:g.9343450G>C (hg19) ; chr16:g.9249593G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249593G>C , CM000678.2:g.9249593G>C	GRCh38
NC_000016.9:g.9343450G>C , CM000678.1:g.9343450G>C	GRCh37
NC_000016.8:g.9250951G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64860G>C