Canonical Allele Identifier: CA1064137045
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1718658772
gnomAD v3: 4-73404198-C-G
gnomAD v4: 4-73404198-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404198C>G , CM000666.2:g.73404198C>G GRCh38
NC_000004.11:g.74269915C>G , CM000666.1:g.74269915C>G GRCh37
NC_000004.10:g.74488779C>G NCBI36
NG_009291.1:g.4944C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-171C>G ENSP00000392541.1:n.48-171C>G