Canonical Allele Identifier: CA217115782

Gene: HBB

Linked Data

• dbSNP Id: rs33981098
• MyVariant Identifiers: chr11:g.5248332T>G (hg19) ; chr11:g.5227102T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5227102T>G , CM000673.2:g.5227102T>G	GRCh38
NC_000011.9:g.5248332T>G , CM000673.1:g.5248332T>G	GRCh37
NC_000011.8:g.5204908T>G	NCBI36
NG_000007.3:g.70514A>C
NG_059281.1:g.4970A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647020.1:c.-81A>C	ENSP00000494175.1:n.-81A>C
ENST00000380315.2:c.-18-63A>C	ENSP00000369671.2:n.-18-63A>C