Canonical Allele Identifier: CA55082055

Gene:

Linked Data

• dbSNP Id: rs879878030
• gnomAD v2: 2-123641683-T-G
• gnomAD v3: 2-122884107-T-G
• gnomAD v4: 2-122884107-T-G
• MyVariant Identifiers: chr2:g.123641683T>G (hg19) ; chr2:g.122884107T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122884107T>G , CM000664.2:g.122884107T>G	GRCh38
NC_000002.11:g.123641683T>G , CM000664.1:g.123641683T>G	GRCh37
NC_000002.10:g.123358153T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923292.1:n.1125-835T>G
XR_001739692.1:n.1451-835T>G
XR_923292.2:n.1358-835T>G