Canonical Allele Identifier: CA427349507

Gene:

Linked Data

• gnomAD v4: 2-88016425-T-G
• MyVariant Identifiers: chr2:g.88315944T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016425T>G , CM000664.2:g.88016425T>G	GRCh38
NC_000002.11:g.88315944T>G , CM000664.1:g.88315944T>G	GRCh37
NC_000002.10:g.88097059T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.770T>G
XR_940336.3:n.770T>G