Canonical Allele Identifier: CA217118990

Gene: HBG1 HBG2

Linked Data

• dbSNP Id: rs1044043206
• gnomAD v3: 11-5249852-G-A
• gnomAD v4: 11-5249852-G-A
• MyVariant Identifiers: chr11:g.5271082G>A (hg19) ; chr11:g.5249852G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249852G>A , CM000673.2:g.5249852G>A	GRCh38
NC_000011.9:g.5271082G>A , CM000673.1:g.5271082G>A	GRCh37
NC_000011.8:g.5227658G>A	NCBI36
NG_000007.3:g.47764C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.-48C>T (HBG1) MANE Select	ENSP00000327431.4:n.-48C>T
ENST00000642908.1:c.316-1365C>T	ENSP00000495346.1:n.316-1365C>T
ENST00000647543.1:c.379-1365C>T	ENSP00000496470.1:n.379-1365C>T
ENST00000648735.1:n.4C>T (HBG1)
ENST00000330597.3:c.-48C>T (HBG1)	ENSP00000327431.3:n.-48C>T
ENST00000620888.4:c.316-1365C>T (HBG2)	ENSP00000479637.1:n.316-1365C>T
ENST00000623781.1:c.405G>A	ENSP00000485381.1:p.Ala135=
NM_000559.2:c.-48C>T (HBG1)	NP_000550.2:n.-48C>T
NM_000559.3:c.-48C>T (HBG1) MANE Select	NP_000550.2:n.-48C>T