Canonical Allele Identifier: CA54965530

Gene:

Linked Data

• dbSNP Id: rs778632713
• MyVariant Identifiers: chr2:g.123126898_123126899del (hg19) ; chr2:g.122369322_122369323del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122369323_122369324del , CM000664.2:g.122369323_122369324del	GRCh38
NC_000002.11:g.123126899_123126900del , CM000664.1:g.123126899_123126900del	GRCh37
NC_000002.10:g.122843369_122843370del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-23640_556-23639del
XR_001739684.1:n.556-23640_556-23639del