Canonical Allele Identifier: CA2959308

Gene: ALB

Linked Data

• dbSNP Id: rs372694396
• ExAC: 4:74272347 G / A
• gnomAD v2: 4-74272347-G-A
• gnomAD v4: 4-73406630-G-A
• MyVariant Identifiers: chr4:g.74272347G>A (hg19) ; chr4:g.73406630G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406630G>A , CM000666.2:g.73406630G>A	GRCh38
NC_000004.11:g.74272347G>A , CM000666.1:g.74272347G>A	GRCh37
NC_000004.10:g.74491211G>A	NCBI36
NG_009291.1:g.7376G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.139G>A MANE Select	ENSP00000295897.4:p.Val47Met
ENST00000295897.8:c.139G>A	ENSP00000295897.4:p.Val47Met
ENST00000401494.7:c.137+1457G>A	ENSP00000384695.3:n.137+1457G>A
ENST00000415165.6:c.137+1457G>A	ENSP00000401820.2:n.137+1457G>A
ENST00000441319.5:c.145G>A	ENSP00000392541.1:p.Val49Met
ENST00000476441.6:c.79+2224G>A	ENSP00000423727.1:n.79+2224G>A
ENST00000503124.5:c.-100G>A	ENSP00000421027.1:n.-100G>A
ENST00000509063.5:c.139G>A	ENSP00000422784.1:p.Val47Met
ENST00000510166.5:n.175G>A
ENST00000514786.1:n.108G>A
ENST00000515133.5:n.180G>A
ENST00000621085.4:c.139G>A	ENSP00000483421.1:p.Val47Met
ENST00000621628.4:c.139G>A	ENSP00000480485.1:p.Val47Met
NM_000477.5:c.139G>A	NP_000468.1:p.Val47Met
NM_000477.6:c.139G>A	NP_000468.1:p.Val47Met
NM_000477.7:c.139G>A MANE Select	NP_000468.1:p.Val47Met