Canonical Allele Identifier: CA99699102

Gene: ALB

Linked Data

• dbSNP Id: rs967161108
• gnomAD v2: 4-74272857-T-A
• gnomAD v3: 4-73407140-T-A
• gnomAD v4: 4-73407140-T-A
• MyVariant Identifiers: chr4:g.74272857T>A (hg19) ; chr4:g.73407140T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73407140T>A , CM000666.2:g.73407140T>A	GRCh38
NC_000004.11:g.74272857T>A , CM000666.1:g.74272857T>A	GRCh37
NC_000004.10:g.74491721T>A	NCBI36
NG_009291.1:g.7886T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+379T>A MANE Select	ENSP00000295897.4:n.270+379T>A
ENST00000295897.8:c.270+379T>A	ENSP00000295897.4:n.270+379T>A
ENST00000401494.7:c.137+1967T>A	ENSP00000384695.3:n.137+1967T>A
ENST00000415165.6:c.137+1967T>A	ENSP00000401820.2:n.137+1967T>A
ENST00000441319.5:c.276+379T>A	ENSP00000392541.1:n.276+379T>A
ENST00000476441.6:c.80-2215T>A	ENSP00000423727.1:n.80-2215T>A
ENST00000503124.5:c.32+379T>A	ENSP00000421027.1:n.32+379T>A
ENST00000509063.5:c.270+379T>A	ENSP00000422784.1:n.270+379T>A
ENST00000510166.5:n.306+379T>A
ENST00000514786.1:n.239+379T>A
ENST00000515133.5:n.311+379T>A
ENST00000621085.4:c.270+379T>A	ENSP00000483421.1:n.270+379T>A
ENST00000621628.4:c.270+379T>A	ENSP00000480485.1:n.270+379T>A
NM_000477.5:c.270+379T>A	NP_000468.1:n.270+379T>A
NM_000477.6:c.270+379T>A	NP_000468.1:n.270+379T>A
NM_000477.7:c.270+379T>A MANE Select	NP_000468.1:n.270+379T>A