Canonical Allele Identifier: CA2578063685
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404267-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404267C>A , CM000666.2:g.73404267C>A GRCh38
NC_000004.11:g.74269984C>A , CM000666.1:g.74269984C>A GRCh37
NC_000004.10:g.74488848C>A NCBI36
NG_009291.1:g.5013C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-61C>A ENSP00000295897.4:n.-61C>A
ENST00000441319.5:c.48-102C>A ENSP00000392541.1:n.48-102C>A
ENST00000621628.4:c.-61C>A ENSP00000480485.1:n.-61C>A
NM_000477.5:c.-61C>A NP_000468.1:n.-61C>A
NM_000477.6:c.-61C>A NP_000468.1:n.-61C>A