Canonical Allele Identifier: CA99712839

Gene: ALB

Linked Data

• dbSNP Id: rs1020627975
• gnomAD v3: 4-73420467-C-A
• gnomAD v4: 4-73420467-C-A
• MyVariant Identifiers: chr4:g.74286184C>A (hg19) ; chr4:g.73420467C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420467C>A , CM000666.2:g.73420467C>A	GRCh38
NC_000004.11:g.74286184C>A , CM000666.1:g.74286184C>A	GRCh37
NC_000004.10:g.74505048C>A	NCBI36
NG_009291.1:g.21213C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*23+146C>A MANE Select	ENSP00000295897.4:n.*23+146C>A
ENST00000295897.8:c.*23+146C>A	ENSP00000295897.4:n.*23+146C>A
ENST00000401494.7:c.*23+146C>A	ENSP00000384695.3:n.*23+146C>A
ENST00000415165.6:c.*23+146C>A	ENSP00000401820.2:n.*23+146C>A
ENST00000476441.6:c.*1132+146C>A	ENSP00000423727.1:n.*1132+146C>A
ENST00000495173.1:n.161+146C>A
ENST00000503124.5:c.*23+146C>A	ENSP00000421027.1:n.*23+146C>A
ENST00000505649.5:n.1400+146C>A
ENST00000508932.5:n.243+146C>A
ENST00000509063.5:c.1786-625C>A	ENSP00000422784.1:n.1786-625C>A
ENST00000511370.1:c.1386+146C>A
ENST00000621085.4:c.*23+146C>A	ENSP00000483421.1:n.*23+146C>A
ENST00000621628.4:c.*23+146C>A	ENSP00000480485.1:n.*23+146C>A
NM_000477.5:c.*23+146C>A	NP_000468.1:n.*23+146C>A
NM_000477.6:c.*23+146C>A	NP_000468.1:n.*23+146C>A
NM_000477.7:c.*23+146C>A MANE Select	NP_000468.1:n.*23+146C>A