Canonical Allele Identifier: CA2959238
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs772076420
ExAC: 4:74269997 G / A
gnomAD v2: 4-74269997-G-A
gnomAD v3: 4-73404280-G-A
gnomAD v4: 4-73404280-G-A
MyVariant Identifiers: chr4:g.74269997G>A (hg19) chr4:g.73404280G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404280G>A , CM000666.2:g.73404280G>A GRCh38
NC_000004.11:g.74269997G>A , CM000666.1:g.74269997G>A GRCh37
NC_000004.10:g.74488861G>A NCBI36
NG_009291.1:g.5026G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.8:c.-48G>A ENSP00000295897.4:n.-48G>A
ENST00000441319.5:c.48-89G>A ENSP00000392541.1:n.48-89G>A
ENST00000621628.4:c.-48G>A ENSP00000480485.1:n.-48G>A
NM_000477.5:c.-48G>A NP_000468.1:n.-48G>A
NM_000477.6:c.-48G>A NP_000468.1:n.-48G>A
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