Canonical Allele Identifier: CA2670936388
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404226-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404226G>C , CM000666.2:g.73404226G>C GRCh38
NC_000004.11:g.74269943G>C , CM000666.1:g.74269943G>C GRCh37
NC_000004.10:g.74488807G>C NCBI36
NG_009291.1:g.4972G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-143G>C ENSP00000392541.1:n.48-143G>C