Canonical Allele Identifier: CA379263422
Gene: HBG1 HGNC NCBI
HBG2 HGNC NCBI

Linked Data

gnomAD v4: 11-5249845-C-T
MyVariant Identifiers: chr11:g.5271075C>T (hg19) chr11:g.5249845C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249845C>T , CM000673.2:g.5249845C>T GRCh38
NC_000011.9:g.5271075C>T , CM000673.1:g.5271075C>T GRCh37
NC_000011.8:g.5227651C>T NCBI36
NG_000007.3:g.47771G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330597.5:c.-41G>A (HBG1) MANE Select ENSP00000327431.4:n.-41G>A
ENST00000642908.1:c.316-1358G>A ENSP00000495346.1:n.316-1358G>A
ENST00000647543.1:c.379-1358G>A ENSP00000496470.1:n.379-1358G>A
ENST00000648735.1:n.11G>A (HBG1)
ENST00000330597.3:c.-41G>A (HBG1) ENSP00000327431.3:n.-41G>A
ENST00000620888.4:c.316-1358G>A (HBG2) ENSP00000479637.1:n.316-1358G>A
ENST00000623781.1:c.398C>T ENSP00000485381.1:p.Pro133Leu
NM_000559.2:c.-41G>A (HBG1) NP_000550.2:n.-41G>A
NM_000559.3:c.-41G>A (HBG1) MANE Select NP_000550.2:n.-41G>A
Search 100 bp 5'
Search 100 bp 3'