Canonical Allele Identifier: CA281436471

Gene:

Linked Data

• dbSNP Id: rs1000533118
• MyVariant Identifiers: chr16:g.55689404A>C (hg19) ; chr16:g.55655492A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55655492A>C , CM000678.2:g.55655492A>C	GRCh38
NC_000016.9:g.55689404A>C , CM000678.1:g.55689404A>C	GRCh37
NC_000016.8:g.54246905A>C	NCBI36
NG_016969.1:g.4863A>C

Transcript Alleles

HGVS	Amino-acid change
XR_933603.1:n.54+107T>G