Canonical Allele Identifier: CA99696150
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs552459263
gnomAD v2: 4-74269831-A-G
gnomAD v3: 4-73404114-A-G
gnomAD v4: 4-73404114-A-G
MyVariant Identifiers: chr4:g.74269831A>G (hg19) chr4:g.73404114A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404114A>G , CM000666.2:g.73404114A>G GRCh38
NC_000004.11:g.74269831A>G , CM000666.1:g.74269831A>G GRCh37
NC_000004.10:g.74488695A>G NCBI36
NG_009291.1:g.4860A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-255A>G ENSP00000392541.1:n.48-255A>G
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