Canonical Allele Identifier: CA2670936426
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404280-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404280G>T , CM000666.2:g.73404280G>T GRCh38
NC_000004.11:g.74269997G>T , CM000666.1:g.74269997G>T GRCh37
NC_000004.10:g.74488861G>T NCBI36
NG_009291.1:g.5026G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-48G>T ENSP00000295897.4:n.-48G>T
ENST00000441319.5:c.48-89G>T ENSP00000392541.1:n.48-89G>T
ENST00000621628.4:c.-48G>T ENSP00000480485.1:n.-48G>T
NM_000477.5:c.-48G>T NP_000468.1:n.-48G>T
NM_000477.6:c.-48G>T NP_000468.1:n.-48G>T