Canonical Allele Identifier: CA798282624
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1402064612
gnomAD v3: 4-73404243-A-G
gnomAD v4: 4-73404243-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404243A>G , CM000666.2:g.73404243A>G GRCh38
NC_000004.11:g.74269960A>G , CM000666.1:g.74269960A>G GRCh37
NC_000004.10:g.74488824A>G NCBI36
NG_009291.1:g.4989A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-85A>G ENSP00000295897.4:n.-85A>G
ENST00000441319.5:c.48-126A>G ENSP00000392541.1:n.48-126A>G
NM_000477.6:c.-85A>G NP_000468.1:n.-85A>G