Canonical Allele Identifier: CA357244918

Gene: ALB

Linked Data

• dbSNP Id: rs1719066702
• MyVariant Identifiers: chr4:g.74283953T>G (hg19) ; chr4:g.73418236T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418236T>G , CM000666.2:g.73418236T>G	GRCh38
NC_000004.11:g.74283953T>G , CM000666.1:g.74283953T>G	GRCh37
NC_000004.10:g.74502817T>G	NCBI36
NG_009291.1:g.18982T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1577T>G MANE Select	ENSP00000295897.4:p.Phe526Cys
ENST00000295897.8:c.1577T>G	ENSP00000295897.4:p.Phe526Cys
ENST00000401494.7:c.1232T>G	ENSP00000384695.3:p.Phe411Cys
ENST00000415165.6:c.1001T>G	ENSP00000401820.2:p.Phe334Cys
ENST00000476441.6:c.*856T>G	ENSP00000423727.1:n.*856T>G
ENST00000486939.1:n.231T>G
ENST00000503124.5:c.1127T>G	ENSP00000421027.1:p.Phe376Cys
ENST00000505649.5:n.1124T>G
ENST00000509063.5:c.1577T>G	ENSP00000422784.1:p.Phe526Cys
ENST00000511370.1:c.1110T>G
ENST00000621085.4:c.938T>G	ENSP00000483421.1:p.Phe313Cys
ENST00000621628.4:c.938T>G	ENSP00000480485.1:p.Phe313Cys
NM_000477.5:c.1577T>G	NP_000468.1:p.Phe526Cys
NM_000477.6:c.1577T>G	NP_000468.1:p.Phe526Cys
NM_000477.7:c.1577T>G MANE Select	NP_000468.1:p.Phe526Cys