Canonical Allele Identifier: CA379273756
Gene: HBB HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.5246956G>T (hg19) chr11:g.5225726G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225726G>T , CM000673.2:g.5225726G>T GRCh38
NC_000011.9:g.5246956G>T , CM000673.1:g.5246956G>T GRCh37
NC_000011.8:g.5203532G>T NCBI36
NG_000007.3:g.71890C>A
NG_059281.1:g.6346C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.316C>A ENSP00000494175.1:p.Leu106Ile
ENST00000335295.4:c.316C>A MANE Select ENSP00000333994.3:p.Leu106Ile
ENST00000475226.1:n.248C>A
ENST00000633227.1:c.*132C>A ENSP00000488004.1:n.*132C>A
NM_000518.4:c.316C>A NP_000509.1:p.Leu106Ile
NM_000518.5:c.316C>A MANE Select NP_000509.1:p.Leu106Ile
Search 100 bp 5'
Search 100 bp 3'