Canonical Allele Identifier: CA2670936881

Gene: ALB

Linked Data

• gnomAD v4: 4-73406862-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406862C>T , CM000666.2:g.73406862C>T	GRCh38
NC_000004.11:g.74272579C>T , CM000666.1:g.74272579C>T	GRCh37
NC_000004.10:g.74491443C>T	NCBI36
NG_009291.1:g.7608C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+101C>T MANE Select	ENSP00000295897.4:n.270+101C>T
ENST00000295897.8:c.270+101C>T	ENSP00000295897.4:n.270+101C>T
ENST00000401494.7:c.137+1689C>T	ENSP00000384695.3:n.137+1689C>T
ENST00000415165.6:c.137+1689C>T	ENSP00000401820.2:n.137+1689C>T
ENST00000441319.5:c.276+101C>T	ENSP00000392541.1:n.276+101C>T
ENST00000476441.6:c.79+2456C>T	ENSP00000423727.1:n.79+2456C>T
ENST00000503124.5:c.32+101C>T	ENSP00000421027.1:n.32+101C>T
ENST00000509063.5:c.270+101C>T	ENSP00000422784.1:n.270+101C>T
ENST00000510166.5:n.306+101C>T
ENST00000514786.1:n.239+101C>T
ENST00000515133.5:n.311+101C>T
ENST00000621085.4:c.270+101C>T	ENSP00000483421.1:n.270+101C>T
ENST00000621628.4:c.270+101C>T	ENSP00000480485.1:n.270+101C>T
NM_000477.5:c.270+101C>T	NP_000468.1:n.270+101C>T
NM_000477.6:c.270+101C>T	NP_000468.1:n.270+101C>T
NM_000477.7:c.270+101C>T MANE Select	NP_000468.1:n.270+101C>T