Canonical Allele Identifier: CA472885708
Gene: HBB HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.5248216A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226986A>C , CM000673.2:g.5226986A>C GRCh38
NC_000011.9:g.5248216A>C , CM000673.1:g.5248216A>C GRCh37
NC_000011.8:g.5204792A>C NCBI36
NG_000007.3:g.70630T>G
NG_059281.1:g.5086T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.36T>G ENSP00000494175.1:p.Val12=
ENST00000335295.4:c.36T>G MANE Select ENSP00000333994.3:p.Val12=
ENST00000380315.2:c.36T>G ENSP00000369671.2:p.Val12=
ENST00000485743.1:n.87T>G
ENST00000633227.1:c.36T>G ENSP00000488004.1:p.Val12=
NM_000518.4:c.36T>G NP_000509.1:p.Val12=
NM_000518.5:c.36T>G MANE Select NP_000509.1:p.Val12=
Search 100 bp 5'
Search 100 bp 3'