Canonical Allele Identifier: CA1468148386
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404283T= , CM000666.2:g.73404283T= GRCh38
NC_000004.11:g.74270000T= , CM000666.1:g.74270000T= GRCh37
NC_000004.10:g.74488864T= NCBI36
NG_009291.1:g.5029T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.8:c.-45T= ENSP00000295897.4:n.-45T=
ENST00000441319.5:c.48-86T= ENSP00000392541.1:n.48-86T=
ENST00000621628.4:c.-45T= ENSP00000480485.1:n.-45T=
NM_000477.5:c.-45T= NP_000468.1:n.-45T=
NM_000477.6:c.-45T= NP_000468.1:n.-45T=