Canonical Allele Identifier: CA54965519

Gene:

Linked Data

• dbSNP Id: rs773450660
• MyVariant Identifiers: chr2:g.123126816_123126823del (hg19) ; chr2:g.122369240_122369247del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122369240_122369247del , CM000664.2:g.122369240_122369247del	GRCh38
NC_000002.11:g.123126816_123126823del , CM000664.1:g.123126816_123126823del	GRCh37
NC_000002.10:g.122843286_122843293del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-23723_556-23716del
XR_001739684.1:n.556-23723_556-23716del