Canonical Allele Identifier: CA5840162

Linked Data

dbSNP Id: rs527266118
gnomAD v2: 11-5270630-C-T
gnomAD v3: 11-5249400-C-T
gnomAD v4: 11-5249400-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249400C>T , CM000673.2:g.5249400C>T GRCh38
NC_000011.9:g.5270630C>T , CM000673.1:g.5270630C>T GRCh37
NC_000011.8:g.5227206C>T NCBI36
NG_000007.3:g.48216G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000330597.5:c.283G>A (HBG1) MANE Select ENSP00000327431.4:p.Asp95Asn
ENST00000642908.1:c.316-913G>A ENSP00000495346.1:n.316-913G>A
ENST00000647543.1:c.379-913G>A ENSP00000496470.1:n.379-913G>A
ENST00000648735.1:n.334G>A (HBG1)
ENST00000330597.3:c.283G>A (HBG1) ENSP00000327431.3:p.Asp95Asn
ENST00000620888.4:c.316-913G>A (HBG2) ENSP00000479637.1:n.316-913G>A
ENST00000623781.1:c.72C>T ENSP00000485381.1:p.Val24=
ENST00000632727.1:c.*152G>A (HBG1) ENSP00000488759.1:n.*152G>A
NM_000559.2:c.283G>A (HBG1) NP_000550.2:p.Asp95Asn
NM_000559.3:c.283G>A (HBG1) MANE Select NP_000550.2:p.Asp95Asn