Canonical Allele Identifier: CA756174455

Gene:

Linked Data

• dbSNP Id: rs1255395698
• gnomAD v3: 2-122369106-TATC-T
• gnomAD v4: 2-122369106-TATC-T
• MyVariant Identifiers: chr2:g.123126683_123126685del (hg19) ; chr2:g.122369107_122369109del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122369109_122369111del , CM000664.2:g.122369109_122369111del	GRCh38
NC_000002.11:g.123126685_123126687del , CM000664.1:g.123126685_123126687del	GRCh37
NC_000002.10:g.122843155_122843157del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-23854_556-23852del
XR_001739684.1:n.556-23854_556-23852del