Canonical Allele Identifier: CA439948397

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283942T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418225T>G , CM000666.2:g.73418225T>G	GRCh38
NC_000004.11:g.74283942T>G , CM000666.1:g.74283942T>G	GRCh37
NC_000004.10:g.74502806T>G	NCBI36
NG_009291.1:g.18971T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1566T>G MANE Select	ENSP00000295897.4:p.Val522=
ENST00000295897.8:c.1566T>G	ENSP00000295897.4:p.Val522=
ENST00000401494.7:c.1221T>G	ENSP00000384695.3:p.Val407=
ENST00000415165.6:c.990T>G	ENSP00000401820.2:p.Val330=
ENST00000476441.6:c.*845T>G	ENSP00000423727.1:n.*845T>G
ENST00000486939.1:n.220T>G
ENST00000503124.5:c.1116T>G	ENSP00000421027.1:p.Val372=
ENST00000505649.5:n.1113T>G
ENST00000509063.5:c.1566T>G	ENSP00000422784.1:p.Val522=
ENST00000511370.1:c.1099T>G
ENST00000621085.4:c.927T>G	ENSP00000483421.1:p.Val309=
ENST00000621628.4:c.927T>G	ENSP00000480485.1:p.Val309=
NM_000477.5:c.1566T>G	NP_000468.1:p.Val522=
NM_000477.6:c.1566T>G	NP_000468.1:p.Val522=
NM_000477.7:c.1566T>G MANE Select	NP_000468.1:p.Val522=