Canonical Allele Identifier: CA2521750389
Gene: ALB HGNC NCBI
gnomAD v4:
chr4-73404133-T-C
Joint Max Group AF 0.00000109 (NFE)
Exomes Max Group AF 0.0000014 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404133T>C , CM000666.2:g.73404133T>C GRCh38
NC_000004.11:g.74269850T>C , CM000666.1:g.74269850T>C GRCh37
NC_000004.10:g.74488714T>C NCBI36
NG_009291.1:g.4879T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-236T>C ENSP00000392541.1:n.48-236T>C
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