Canonical Allele Identifier: CA439948329

Gene: ALB

Linked Data

• dbSNP Id: rs778288086
• gnomAD v2: 4-74283828-A-G
• gnomAD v3: 4-73418111-A-G
• gnomAD v4: 4-73418111-A-G
• MyVariant Identifiers: chr4:g.74283828A>G (hg19) ; chr4:g.73418111A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418111A>G , CM000666.2:g.73418111A>G	GRCh38
NC_000004.11:g.74283828A>G , CM000666.1:g.74283828A>G	GRCh37
NC_000004.10:g.74502692A>G	NCBI36
NG_009291.1:g.18857A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1452A>G MANE Select	ENSP00000295897.4:p.Leu484=
ENST00000295897.8:c.1452A>G	ENSP00000295897.4:p.Leu484=
ENST00000401494.7:c.1107A>G	ENSP00000384695.3:p.Leu369=
ENST00000415165.6:c.876A>G	ENSP00000401820.2:p.Leu292=
ENST00000476441.6:c.*731A>G	ENSP00000423727.1:n.*731A>G
ENST00000486939.1:n.106A>G
ENST00000503124.5:c.1002A>G	ENSP00000421027.1:p.Leu334=
ENST00000505649.5:n.999A>G
ENST00000509063.5:c.1452A>G	ENSP00000422784.1:p.Leu484=
ENST00000511370.1:c.985A>G
ENST00000621085.4:c.813A>G	ENSP00000483421.1:p.Leu271=
ENST00000621628.4:c.813A>G	ENSP00000480485.1:p.Leu271=
NM_000477.5:c.1452A>G	NP_000468.1:p.Leu484=
NM_000477.6:c.1452A>G	NP_000468.1:p.Leu484=
NM_000477.7:c.1452A>G MANE Select	NP_000468.1:p.Leu484=