Canonical Allele Identifier: CA2670936313
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404111-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404111G>T , CM000666.2:g.73404111G>T GRCh38
NC_000004.11:g.74269828G>T , CM000666.1:g.74269828G>T GRCh37
NC_000004.10:g.74488692G>T NCBI36
NG_009291.1:g.4857G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-258G>T ENSP00000392541.1:n.48-258G>T
Search 100 bp 5'
Search 100 bp 3'