Canonical Allele Identifier: CA2578063680
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404254A>T , CM000666.2:g.73404254A>T GRCh38
NC_000004.11:g.74269971A>T , CM000666.1:g.74269971A>T GRCh37
NC_000004.10:g.74488835A>T NCBI36
NG_009291.1:g.5000A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-74A>T ENSP00000295897.4:n.-74A>T
ENST00000441319.5:c.48-115A>T ENSP00000392541.1:n.48-115A>T
NM_000477.6:c.-74A>T NP_000468.1:n.-74A>T