Canonical Allele Identifier: CA1468141876

Gene: ALB

Linked Data

• dbSNP Id: rs1718926396

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413358T>G , CM000666.2:g.73413358T>G	GRCh38
NC_000004.11:g.74279075T>G , CM000666.1:g.74279075T>G	GRCh37
NC_000004.10:g.74497939T>G	NCBI36
NG_009291.1:g.14104T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.844-62T>G MANE Select	ENSP00000295897.4:n.844-62T>G
ENST00000295897.8:c.844-62T>G	ENSP00000295897.4:n.844-62T>G
ENST00000401494.7:c.499-62T>G	ENSP00000384695.3:n.499-62T>G
ENST00000415165.6:c.268-62T>G	ENSP00000401820.2:n.268-62T>G
ENST00000476441.6:c.*123-62T>G	ENSP00000423727.1:n.*123-62T>G
ENST00000484992.1:n.102T>G
ENST00000503124.5:c.394-62T>G	ENSP00000421027.1:n.394-62T>G
ENST00000505649.5:n.530-62T>G
ENST00000509063.5:c.844-62T>G	ENSP00000422784.1:n.844-62T>G
ENST00000511370.1:c.377-62T>G
ENST00000621085.4:c.491-1748T>G	ENSP00000483421.1:n.491-1748T>G
ENST00000621628.4:c.487-1744T>G	ENSP00000480485.1:n.487-1744T>G
NM_000477.5:c.844-62T>G	NP_000468.1:n.844-62T>G
NM_000477.6:c.844-62T>G	NP_000468.1:n.844-62T>G
NM_000477.7:c.844-62T>G MANE Select	NP_000468.1:n.844-62T>G