Canonical Allele Identifier: CA439948343

Gene: ALB

Linked Data

• dbSNP Id: rs775238949
• MyVariant Identifiers: chr4:g.74283855A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418138A>C , CM000666.2:g.73418138A>C	GRCh38
NC_000004.11:g.74283855A>C , CM000666.1:g.74283855A>C	GRCh37
NC_000004.10:g.74502719A>C	NCBI36
NG_009291.1:g.18884A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1479A>C MANE Select	ENSP00000295897.4:p.Val493=
ENST00000295897.8:c.1479A>C	ENSP00000295897.4:p.Val493=
ENST00000401494.7:c.1134A>C	ENSP00000384695.3:p.Val378=
ENST00000415165.6:c.903A>C	ENSP00000401820.2:p.Val301=
ENST00000476441.6:c.*758A>C	ENSP00000423727.1:n.*758A>C
ENST00000486939.1:n.133A>C
ENST00000503124.5:c.1029A>C	ENSP00000421027.1:p.Val343=
ENST00000505649.5:n.1026A>C
ENST00000509063.5:c.1479A>C	ENSP00000422784.1:p.Val493=
ENST00000511370.1:c.1012A>C
ENST00000621085.4:c.840A>C	ENSP00000483421.1:p.Val280=
ENST00000621628.4:c.840A>C	ENSP00000480485.1:p.Val280=
NM_000477.5:c.1479A>C	NP_000468.1:p.Val493=
NM_000477.6:c.1479A>C	NP_000468.1:p.Val493=
NM_000477.7:c.1479A>C MANE Select	NP_000468.1:p.Val493=