Canonical Allele Identifier: CA934688347
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs1847593170
gnomAD v3: 11-5227176-G-A
gnomAD v4: 11-5227176-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227176G>A , CM000673.2:g.5227176G>A GRCh38
NC_000011.9:g.5248406G>A , CM000673.1:g.5248406G>A GRCh37
NC_000011.8:g.5204982G>A NCBI36
NG_000007.3:g.70440C>T
NG_059281.1:g.4896C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-155C>T ENSP00000494175.1:n.-155C>T
ENST00000380315.2:c.-18-137C>T ENSP00000369671.2:n.-18-137C>T