Canonical Allele Identifier: CA2670936325
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404137-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404137C>T , CM000666.2:g.73404137C>T GRCh38
NC_000004.11:g.74269854C>T , CM000666.1:g.74269854C>T GRCh37
NC_000004.10:g.74488718C>T NCBI36
NG_009291.1:g.4883C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-232C>T ENSP00000392541.1:n.48-232C>T