Canonical Allele Identifier: CA99696149
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs964753624
gnomAD v4: 4-73404100-G-A
MyVariant Identifiers: chr4:g.74269817G>A (hg19) chr4:g.73404100G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404100G>A , CM000666.2:g.73404100G>A GRCh38
NC_000004.11:g.74269817G>A , CM000666.1:g.74269817G>A GRCh37
NC_000004.10:g.74488681G>A NCBI36
NG_009291.1:g.4846G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-269G>A ENSP00000392541.1:n.48-269G>A
Search 100 bp 5'
Search 100 bp 3'