Canonical Allele Identifier: CA99710407

Gene: ALB

Linked Data

• dbSNP Id: rs755880314
• gnomAD v4: 4-73418145-A-C
• MyVariant Identifiers: chr4:g.74283862A>C (hg19) ; chr4:g.73418145A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418145A>C , CM000666.2:g.73418145A>C	GRCh38
NC_000004.11:g.74283862A>C , CM000666.1:g.74283862A>C	GRCh37
NC_000004.10:g.74502726A>C	NCBI36
NG_009291.1:g.18891A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1486A>C MANE Select	ENSP00000295897.4:p.Arg496=
ENST00000295897.8:c.1486A>C	ENSP00000295897.4:p.Arg496=
ENST00000401494.7:c.1141A>C	ENSP00000384695.3:p.Arg381=
ENST00000415165.6:c.910A>C	ENSP00000401820.2:p.Arg304=
ENST00000476441.6:c.*765A>C	ENSP00000423727.1:n.*765A>C
ENST00000486939.1:n.140A>C
ENST00000503124.5:c.1036A>C	ENSP00000421027.1:p.Arg346=
ENST00000505649.5:n.1033A>C
ENST00000509063.5:c.1486A>C	ENSP00000422784.1:p.Arg496=
ENST00000511370.1:c.1019A>C
ENST00000621085.4:c.847A>C	ENSP00000483421.1:p.Arg283=
ENST00000621628.4:c.847A>C	ENSP00000480485.1:p.Arg283=
NM_000477.5:c.1486A>C	NP_000468.1:p.Arg496=
NM_000477.6:c.1486A>C	NP_000468.1:p.Arg496=
NM_000477.7:c.1486A>C MANE Select	NP_000468.1:p.Arg496=