Canonical Allele Identifier: CA2670936400
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404249dup , CM000666.2:g.73404249dup GRCh38
NC_000004.11:g.74269966dup , CM000666.1:g.74269966dup GRCh37
NC_000004.10:g.74488830dup NCBI36
NG_009291.1:g.4995dup

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-79dup ENSP00000295897.4:n.-79dup
ENST00000441319.5:c.48-120dup ENSP00000392541.1:n.48-120dup
NM_000477.6:c.-79dup NP_000468.1:n.-79dup