Canonical Allele Identifier: CA2578063676
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404249-T-G

Genomic Alleles

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

Transcript Alleles

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