Canonical Allele Identifier: CA99696251
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs907562413
gnomAD v2: 4-74269954-A-C
gnomAD v3: 4-73404237-A-C
gnomAD v4: 4-73404237-A-C
MyVariant Identifiers: chr4:g.74269954A>C (hg19) chr4:g.73404237A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404237A>C , CM000666.2:g.73404237A>C GRCh38
NC_000004.11:g.74269954A>C , CM000666.1:g.74269954A>C GRCh37
NC_000004.10:g.74488818A>C NCBI36
NG_009291.1:g.4983A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-132A>C ENSP00000392541.1:n.48-132A>C
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