Canonical Allele Identifier: CA217115897
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs1013465391
MyVariant Identifiers: chr11:g.5248440G>C (hg19) chr11:g.5227210G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227210G>C , CM000673.2:g.5227210G>C GRCh38
NC_000011.9:g.5248440G>C , CM000673.1:g.5248440G>C GRCh37
NC_000011.8:g.5205016G>C NCBI36
NG_000007.3:g.70406C>G
NG_059281.1:g.4862C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380315.2:c.-18-171C>G ENSP00000369671.2:n.-18-171C>G
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