Canonical Allele Identifier: CA2579829072
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5227025-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227025G>T , CM000673.2:g.5227025G>T GRCh38
NC_000011.9:g.5248255G>T , CM000673.1:g.5248255G>T GRCh37
NC_000011.8:g.5204831G>T NCBI36
NG_000007.3:g.70591C>A
NG_059281.1:g.5047C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-4C>A ENSP00000494175.1:n.-4C>A
ENST00000335295.4:c.-4C>A MANE Select ENSP00000333994.3:n.-4C>A
ENST00000380315.2:c.-4C>A ENSP00000369671.2:n.-4C>A
ENST00000485743.1:n.48C>A
ENST00000633227.1:c.-4C>A ENSP00000488004.1:n.-4C>A
NM_000518.4:c.-4C>A NP_000509.1:n.-4C>A
NM_000518.5:c.-4C>A MANE Select NP_000509.1:n.-4C>A
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