Canonical Allele Identifier: CA99696091
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1011962043
gnomAD v2: 4-74269789-G-A
gnomAD v3: 4-73404072-G-A
gnomAD v4: 4-73404072-G-A
MyVariant Identifiers: chr4:g.74269789G>A (hg19) chr4:g.73404072G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404072G>A , CM000666.2:g.73404072G>A GRCh38
NC_000004.11:g.74269789G>A , CM000666.1:g.74269789G>A GRCh37
NC_000004.10:g.74488653G>A NCBI36
NG_009291.1:g.4818G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-297G>A ENSP00000392541.1:n.48-297G>A
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