Canonical Allele Identifier: CA439948339

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283849G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418132G>C , CM000666.2:g.73418132G>C	GRCh38
NC_000004.11:g.74283849G>C , CM000666.1:g.74283849G>C	GRCh37
NC_000004.10:g.74502713G>C	NCBI36
NG_009291.1:g.18878G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1473G>C MANE Select	ENSP00000295897.4:p.Thr491=
ENST00000295897.8:c.1473G>C	ENSP00000295897.4:p.Thr491=
ENST00000401494.7:c.1128G>C	ENSP00000384695.3:p.Thr376=
ENST00000415165.6:c.897G>C	ENSP00000401820.2:p.Thr299=
ENST00000476441.6:c.*752G>C	ENSP00000423727.1:n.*752G>C
ENST00000486939.1:n.127G>C
ENST00000503124.5:c.1023G>C	ENSP00000421027.1:p.Thr341=
ENST00000505649.5:n.1020G>C
ENST00000509063.5:c.1473G>C	ENSP00000422784.1:p.Thr491=
ENST00000511370.1:c.1006G>C
ENST00000621085.4:c.834G>C	ENSP00000483421.1:p.Thr278=
ENST00000621628.4:c.834G>C	ENSP00000480485.1:p.Thr278=
NM_000477.5:c.1473G>C	NP_000468.1:p.Thr491=
NM_000477.6:c.1473G>C	NP_000468.1:p.Thr491=
NM_000477.7:c.1473G>C MANE Select	NP_000468.1:p.Thr491=