Canonical Allele Identifier: CA2578063681
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404255-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404255A>C , CM000666.2:g.73404255A>C GRCh38
NC_000004.11:g.74269972A>C , CM000666.1:g.74269972A>C GRCh37
NC_000004.10:g.74488836A>C NCBI36
NG_009291.1:g.5001A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-73A>C ENSP00000295897.4:n.-73A>C
ENST00000441319.5:c.48-114A>C ENSP00000392541.1:n.48-114A>C
ENST00000621628.4:c.-73A>C ENSP00000480485.1:n.-73A>C
NM_000477.5:c.-73A>C NP_000468.1:n.-73A>C
NM_000477.6:c.-73A>C NP_000468.1:n.-73A>C