Canonical Allele Identifier: CA281436470

Gene:

Linked Data

• dbSNP Id: rs545583983
• gnomAD v3: 16-55655484-G-A
• gnomAD v4: 16-55655484-G-A
• MyVariant Identifiers: chr16:g.55689396G>A (hg19) ; chr16:g.55655484G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55655484G>A , CM000678.2:g.55655484G>A	GRCh38
NC_000016.9:g.55689396G>A , CM000678.1:g.55689396G>A	GRCh37
NC_000016.8:g.54246897G>A	NCBI36
NG_016969.1:g.4855G>A

Transcript Alleles

HGVS	Amino-acid change
XR_933603.1:n.54+115C>T