Canonical Allele Identifier: CA99698893

Gene: ALB

Linked Data

• dbSNP Id: rs1033518390
• gnomAD v2: 4-74272624-C-G
• gnomAD v3: 4-73406907-C-G
• gnomAD v4: 4-73406907-C-G
• MyVariant Identifiers: chr4:g.74272624C>G (hg19) ; chr4:g.73406907C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406907C>G , CM000666.2:g.73406907C>G	GRCh38
NC_000004.11:g.74272624C>G , CM000666.1:g.74272624C>G	GRCh37
NC_000004.10:g.74491488C>G	NCBI36
NG_009291.1:g.7653C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+146C>G MANE Select	ENSP00000295897.4:n.270+146C>G
ENST00000295897.8:c.270+146C>G	ENSP00000295897.4:n.270+146C>G
ENST00000401494.7:c.137+1734C>G	ENSP00000384695.3:n.137+1734C>G
ENST00000415165.6:c.137+1734C>G	ENSP00000401820.2:n.137+1734C>G
ENST00000441319.5:c.276+146C>G	ENSP00000392541.1:n.276+146C>G
ENST00000476441.6:c.80-2448C>G	ENSP00000423727.1:n.80-2448C>G
ENST00000503124.5:c.32+146C>G	ENSP00000421027.1:n.32+146C>G
ENST00000509063.5:c.270+146C>G	ENSP00000422784.1:n.270+146C>G
ENST00000510166.5:n.306+146C>G
ENST00000514786.1:n.239+146C>G
ENST00000515133.5:n.311+146C>G
ENST00000621085.4:c.270+146C>G	ENSP00000483421.1:n.270+146C>G
ENST00000621628.4:c.270+146C>G	ENSP00000480485.1:n.270+146C>G
NM_000477.5:c.270+146C>G	NP_000468.1:n.270+146C>G
NM_000477.6:c.270+146C>G	NP_000468.1:n.270+146C>G
NM_000477.7:c.270+146C>G MANE Select	NP_000468.1:n.270+146C>G