Canonical Allele Identifier: CA99705564

Gene: ALB

Linked Data

• dbSNP Id: rs74718349
• MyVariant Identifiers: chr4:g.74279193G>T (hg19) ; chr4:g.73413476G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413476G>T , CM000666.2:g.73413476G>T	GRCh38
NC_000004.11:g.74279193G>T , CM000666.1:g.74279193G>T	GRCh37
NC_000004.10:g.74498057G>T	NCBI36
NG_009291.1:g.14222G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.900G>T MANE Select	ENSP00000295897.4:p.Lys300Asn
ENST00000295897.8:c.900G>T	ENSP00000295897.4:p.Lys300Asn
ENST00000401494.7:c.555G>T	ENSP00000384695.3:p.Lys185Asn
ENST00000415165.6:c.324G>T	ENSP00000401820.2:p.Lys108Asn
ENST00000476441.6:c.*179G>T	ENSP00000423727.1:n.*179G>T
ENST00000484992.1:n.220G>T
ENST00000503124.5:c.450G>T	ENSP00000421027.1:p.Lys150Asn
ENST00000505649.5:n.586G>T
ENST00000509063.5:c.900G>T	ENSP00000422784.1:p.Lys300Asn
ENST00000511370.1:c.433G>T
ENST00000621085.4:c.491-1630G>T	ENSP00000483421.1:n.491-1630G>T
ENST00000621628.4:c.487-1626G>T	ENSP00000480485.1:n.487-1626G>T
NM_000477.5:c.900G>T	NP_000468.1:p.Lys300Asn
NM_000477.6:c.900G>T	NP_000468.1:p.Lys300Asn
NM_000477.7:c.900G>T MANE Select	NP_000468.1:p.Lys300Asn