Canonical Allele Identifier: CA2670936360
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404187-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404187T>C , CM000666.2:g.73404187T>C GRCh38
NC_000004.11:g.74269904T>C , CM000666.1:g.74269904T>C GRCh37
NC_000004.10:g.74488768T>C NCBI36
NG_009291.1:g.4933T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-182T>C ENSP00000392541.1:n.48-182T>C