Canonical Allele Identifier: CA622292850

Gene:

Linked Data

• dbSNP Id: rs1411037981
• gnomAD v2: 16-55689405-A-G
• gnomAD v3: 16-55655493-A-G
• gnomAD v4: 16-55655493-A-G
• MyVariant Identifiers: chr16:g.55689405A>G (hg19) ; chr16:g.55655493A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55655493A>G , CM000678.2:g.55655493A>G	GRCh38
NC_000016.9:g.55689405A>G , CM000678.1:g.55689405A>G	GRCh37
NC_000016.8:g.54246906A>G	NCBI36
NG_016969.1:g.4864A>G

Transcript Alleles

HGVS	Amino-acid change
XR_933603.1:n.54+106T>C