Canonical Allele Identifier: CA1468148362
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404241T= , CM000666.2:g.73404241T= GRCh38
NC_000004.11:g.74269958T= , CM000666.1:g.74269958T= GRCh37
NC_000004.10:g.74488822T= NCBI36
NG_009291.1:g.4987T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-87T= ENSP00000295897.4:n.-87T=
ENST00000441319.5:c.48-128T= ENSP00000392541.1:n.48-128T=
NM_000477.6:c.-87T= NP_000468.1:n.-87T=