Canonical Allele Identifier: CA2959239
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 349615
ClinVar RCV Id: RCV000312660
dbSNP Id: rs375806262
gnomAD v2: 4-74270000-T-C
gnomAD v3: 4-73404283-T-C
gnomAD v4: 4-73404283-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404283T>C , CM000666.2:g.73404283T>C GRCh38
NC_000004.11:g.74270000T>C , CM000666.1:g.74270000T>C GRCh37
NC_000004.10:g.74488864T>C NCBI36
NG_009291.1:g.5029T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-45T>C ENSP00000295897.4:n.-45T>C
ENST00000441319.5:c.48-86T>C ENSP00000392541.1:n.48-86T>C
ENST00000621628.4:c.-45T>C ENSP00000480485.1:n.-45T>C
NM_000477.5:c.-45T>C NP_000468.1:n.-45T>C
NM_000477.6:c.-45T>C NP_000468.1:n.-45T>C