Canonical Allele Identifier: CA439799172

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274478G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408761G>T , CM000666.2:g.73408761G>T	GRCh38
NC_000004.11:g.74274478G>T , CM000666.1:g.74274478G>T	GRCh37
NC_000004.10:g.74493342G>T	NCBI36
NG_009291.1:g.9507G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.438G>T MANE Select	ENSP00000295897.4:p.Val146=
ENST00000295897.8:c.438G>T	ENSP00000295897.4:p.Val146=
ENST00000401494.7:c.138-594G>T	ENSP00000384695.3:n.138-594G>T
ENST00000415165.6:c.138-3235G>T	ENSP00000401820.2:n.138-3235G>T
ENST00000441319.5:c.444G>T	ENSP00000392541.1:p.Val148=
ENST00000476441.6:c.80-594G>T	ENSP00000423727.1:n.80-594G>T
ENST00000503124.5:c.33-594G>T	ENSP00000421027.1:n.33-594G>T
ENST00000505649.5:n.124G>T
ENST00000509063.5:c.438G>T	ENSP00000422784.1:p.Val146=
ENST00000510166.5:n.474G>T
ENST00000514786.1:n.407G>T
ENST00000515133.5:n.479G>T
ENST00000621085.4:c.438G>T	ENSP00000483421.1:p.Val146=
ENST00000621628.4:c.438G>T	ENSP00000480485.1:p.Val146=
NM_000477.5:c.438G>T	NP_000468.1:p.Val146=
NM_000477.6:c.438G>T	NP_000468.1:p.Val146=
NM_000477.7:c.438G>T MANE Select	NP_000468.1:p.Val146=