Canonical Allele Identifier: CA2739276176

Gene: HBB

Linked Data

• ClinVar Variation Id: 2853365
• ClinVar RCV Id: RCV003695996

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226995_5227524del , CM000673.2:g.5226995_5227524del	GRCh38
NC_000011.9:g.5248225_5248754del , CM000673.1:g.5248225_5248754del	GRCh37
NC_000011.8:g.5204801_5205330del	NCBI36
NG_000007.3:g.70094_70623del
NG_059281.1:g.4550_5079del

Transcript Alleles

HGVS	Amino-acid change
ENST00000380315.2:c.-29_29del