Canonical Allele Identifier: CA1468148320
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404141A= , CM000666.2:g.73404141A= GRCh38
NC_000004.11:g.74269858A= , CM000666.1:g.74269858A= GRCh37
NC_000004.10:g.74488722A= NCBI36
NG_009291.1:g.4887A=

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-228A= ENSP00000392541.1:n.48-228A=