Canonical Allele Identifier: CA99696148
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs527586957
gnomAD v3: 4-73404090-A-C
gnomAD v4: 4-73404090-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404090A>C , CM000666.2:g.73404090A>C GRCh38
NC_000004.11:g.74269807A>C , CM000666.1:g.74269807A>C GRCh37
NC_000004.10:g.74488671A>C NCBI36
NG_009291.1:g.4836A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-279A>C ENSP00000392541.1:n.48-279A>C