Canonical Allele Identifier: CA217115863
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs376350710
MyVariant Identifiers: chr11:g.5248392T>G (hg19) chr11:g.5227162T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227162T>G , CM000673.2:g.5227162T>G GRCh38
NC_000011.9:g.5248392T>G , CM000673.1:g.5248392T>G GRCh37
NC_000011.8:g.5204968T>G NCBI36
NG_000007.3:g.70454A>C
NG_059281.1:g.4910A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-141A>C ENSP00000494175.1:n.-141A>C
ENST00000380315.2:c.-18-123A>C ENSP00000369671.2:n.-18-123A>C
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