Canonical Allele Identifier: CA1468148367
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404247G= , CM000666.2:g.73404247G= GRCh38
NC_000004.11:g.74269964G= , CM000666.1:g.74269964G= GRCh37
NC_000004.10:g.74488828G= NCBI36
NG_009291.1:g.4993G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-81G= ENSP00000295897.4:n.-81G=
ENST00000441319.5:c.48-122G= ENSP00000392541.1:n.48-122G=
NM_000477.6:c.-81G= NP_000468.1:n.-81G=