Canonical Allele Identifier: CA439800285

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280797G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415080G>C , CM000666.2:g.73415080G>C	GRCh38
NC_000004.11:g.74280797G>C , CM000666.1:g.74280797G>C	GRCh37
NC_000004.10:g.74499661G>C	NCBI36
NG_009291.1:g.15826G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1104G>C MANE Select	ENSP00000295897.4:p.Val368=
ENST00000295897.8:c.1104G>C	ENSP00000295897.4:p.Val368=
ENST00000401494.7:c.759G>C	ENSP00000384695.3:p.Val253=
ENST00000415165.6:c.528G>C	ENSP00000401820.2:p.Val176=
ENST00000476441.6:c.*383G>C	ENSP00000423727.1:n.*383G>C
ENST00000484992.1:n.424G>C
ENST00000503124.5:c.654G>C	ENSP00000421027.1:p.Val218=
ENST00000504043.1:n.107G>C
ENST00000505649.5:n.790G>C
ENST00000509063.5:c.1104G>C	ENSP00000422784.1:p.Val368=
ENST00000511370.1:c.637G>C
ENST00000621085.4:c.491-26G>C	ENSP00000483421.1:n.491-26G>C
ENST00000621628.4:c.487-22G>C	ENSP00000480485.1:n.487-22G>C
NM_000477.5:c.1104G>C	NP_000468.1:p.Val368=
NM_000477.6:c.1104G>C	NP_000468.1:p.Val368=
NM_000477.7:c.1104G>C MANE Select	NP_000468.1:p.Val368=