Canonical Allele Identifier: CA206723614

Gene:

Linked Data

• dbSNP Id: rs974757888
• gnomAD v2: 10-43814005-G-A
• gnomAD v3: 10-43318557-G-A
• gnomAD v4: 10-43318557-G-A
• MyVariant Identifiers: chr10:g.43814005G>A (hg19) ; chr10:g.43318557G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43318557G>A , CM000672.2:g.43318557G>A	GRCh38
NC_000010.10:g.43814005G>A , CM000672.1:g.43814005G>A	GRCh37
NC_000010.9:g.43134011G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945902.1:n.70G>A
XR_945902.2:n.160G>A