Canonical Allele Identifier: CA2670936453
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404296-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404296C>A , CM000666.2:g.73404296C>A GRCh38
NC_000004.11:g.74270013C>A , CM000666.1:g.74270013C>A GRCh37
NC_000004.10:g.74488877C>A NCBI36
NG_009291.1:g.5042C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.-32C>A MANE Select ENSP00000295897.4:n.-32C>A
ENST00000295897.8:c.-32C>A ENSP00000295897.4:n.-32C>A
ENST00000415165.6:c.-32C>A ENSP00000401820.2:n.-32C>A
ENST00000441319.5:c.48-73C>A ENSP00000392541.1:n.48-73C>A
ENST00000510166.5:n.10C>A
ENST00000514786.1:n.8C>A
ENST00000515133.5:n.10C>A
ENST00000621085.4:c.-32C>A ENSP00000483421.1:n.-32C>A
ENST00000621628.4:c.-32C>A ENSP00000480485.1:n.-32C>A
NM_000477.5:c.-32C>A NP_000468.1:n.-32C>A
NM_000477.6:c.-32C>A NP_000468.1:n.-32C>A
NM_000477.7:c.-32C>A MANE Select NP_000468.1:n.-32C>A
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