Canonical Allele Identifier: CA2670936403
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404256-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404256G>T , CM000666.2:g.73404256G>T GRCh38
NC_000004.11:g.74269973G>T , CM000666.1:g.74269973G>T GRCh37
NC_000004.10:g.74488837G>T NCBI36
NG_009291.1:g.5002G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-72G>T ENSP00000295897.4:n.-72G>T
ENST00000441319.5:c.48-113G>T ENSP00000392541.1:n.48-113G>T
ENST00000621628.4:c.-72G>T ENSP00000480485.1:n.-72G>T
NM_000477.5:c.-72G>T NP_000468.1:n.-72G>T
NM_000477.6:c.-72G>T NP_000468.1:n.-72G>T