Canonical Allele Identifier: CA2670936349
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404162-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404162T>G , CM000666.2:g.73404162T>G GRCh38
NC_000004.11:g.74269879T>G , CM000666.1:g.74269879T>G GRCh37
NC_000004.10:g.74488743T>G NCBI36
NG_009291.1:g.4908T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-207T>G ENSP00000392541.1:n.48-207T>G