Canonical Allele Identifier: CA439948120

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279181C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413464C>T , CM000666.2:g.73413464C>T	GRCh38
NC_000004.11:g.74279181C>T , CM000666.1:g.74279181C>T	GRCh37
NC_000004.10:g.74498045C>T	NCBI36
NG_009291.1:g.14210C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.888C>T MANE Select	ENSP00000295897.4:p.Ser296=
ENST00000295897.8:c.888C>T	ENSP00000295897.4:p.Ser296=
ENST00000401494.7:c.543C>T	ENSP00000384695.3:p.Ser181=
ENST00000415165.6:c.312C>T	ENSP00000401820.2:p.Ser104=
ENST00000476441.6:c.*167C>T	ENSP00000423727.1:n.*167C>T
ENST00000484992.1:n.208C>T
ENST00000503124.5:c.438C>T	ENSP00000421027.1:p.Ser146=
ENST00000505649.5:n.574C>T
ENST00000509063.5:c.888C>T	ENSP00000422784.1:p.Ser296=
ENST00000511370.1:c.421C>T
ENST00000621085.4:c.491-1642C>T	ENSP00000483421.1:n.491-1642C>T
ENST00000621628.4:c.487-1638C>T	ENSP00000480485.1:n.487-1638C>T
NM_000477.5:c.888C>T	NP_000468.1:p.Ser296=
NM_000477.6:c.888C>T	NP_000468.1:p.Ser296=
NM_000477.7:c.888C>T MANE Select	NP_000468.1:p.Ser296=