Canonical Allele Identifier: CA1468148368
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404251A= , CM000666.2:g.73404251A= GRCh38
NC_000004.11:g.74269968A= , CM000666.1:g.74269968A= GRCh37
NC_000004.10:g.74488832A= NCBI36
NG_009291.1:g.4997A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-77A= ENSP00000295897.4:n.-77A=
ENST00000441319.5:c.48-118A= ENSP00000392541.1:n.48-118A=
NM_000477.6:c.-77A= NP_000468.1:n.-77A=