Canonical Allele Identifier: CA552304185
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1487921035
gnomAD v2: 4-74269844-G-A
gnomAD v3: 4-73404127-G-A
gnomAD v4: 4-73404127-G-A
MyVariant Identifiers: chr4:g.74269844G>A (hg19) chr4:g.73404127G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404127G>A , CM000666.2:g.73404127G>A GRCh38
NC_000004.11:g.74269844G>A , CM000666.1:g.74269844G>A GRCh37
NC_000004.10:g.74488708G>A NCBI36
NG_009291.1:g.4873G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-242G>A ENSP00000392541.1:n.48-242G>A
Search 100 bp 5'
Search 100 bp 3'