Canonical Allele Identifier: CA2579829126
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5227080-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227080G>A , CM000673.2:g.5227080G>A GRCh38
NC_000011.9:g.5248310G>A , CM000673.1:g.5248310G>A GRCh37
NC_000011.8:g.5204886G>A NCBI36
NG_000007.3:g.70536C>T
NG_059281.1:g.4992C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-59C>T ENSP00000494175.1:n.-59C>T
ENST00000380315.2:c.-18-41C>T ENSP00000369671.2:n.-18-41C>T