Canonical Allele Identifier: CA357241248

Gene: ALB

Linked Data

• dbSNP Id: rs1236915932
• gnomAD v2: 4-74280817-A-G
• gnomAD v4: 4-73415100-A-G
• MyVariant Identifiers: chr4:g.74280817A>G (hg19) ; chr4:g.73415100A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415100A>G , CM000666.2:g.73415100A>G	GRCh38
NC_000004.11:g.74280817A>G , CM000666.1:g.74280817A>G	GRCh37
NC_000004.10:g.74499681A>G	NCBI36
NG_009291.1:g.15846A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1124A>G MANE Select	ENSP00000295897.4:p.Lys375Arg
ENST00000295897.8:c.1124A>G	ENSP00000295897.4:p.Lys375Arg
ENST00000401494.7:c.779A>G	ENSP00000384695.3:p.Lys260Arg
ENST00000415165.6:c.548A>G	ENSP00000401820.2:p.Lys183Arg
ENST00000476441.6:c.*403A>G	ENSP00000423727.1:n.*403A>G
ENST00000484992.1:n.444A>G
ENST00000503124.5:c.674A>G	ENSP00000421027.1:p.Lys225Arg
ENST00000504043.1:n.127A>G
ENST00000505649.5:n.810A>G
ENST00000509063.5:c.1124A>G	ENSP00000422784.1:p.Lys375Arg
ENST00000511370.1:c.657A>G
ENST00000621085.4:c.491-6A>G	ENSP00000483421.1:n.491-6A>G
ENST00000621628.4:c.487-2A>G	ENSP00000480485.1:n.487-2A>G
NM_000477.5:c.1124A>G	NP_000468.1:p.Lys375Arg
NM_000477.6:c.1124A>G	NP_000468.1:p.Lys375Arg
NM_000477.7:c.1124A>G MANE Select	NP_000468.1:p.Lys375Arg