Canonical Allele Identifier: CA99696251
Gene: ALB HGNC NCBI
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404237A>C , CM000666.2:g.73404237A>C GRCh38
NC_000004.11:g.74269954A>C , CM000666.1:g.74269954A>C GRCh37
NC_000004.10:g.74488818A>C NCBI36
NG_009291.1:g.4983A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-132A>C ENSP00000392541.1:n.48-132A>C