Canonical Allele Identifier: CA99712412

Gene: ALB

Linked Data

• dbSNP Id: rs562680489
• gnomAD v3: 4-73419943-T-G
• gnomAD v4: 4-73419943-T-G
• MyVariant Identifiers: chr4:g.74285660T>G (hg19) ; chr4:g.73419943T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419943T>G , CM000666.2:g.73419943T>G	GRCh38
NC_000004.11:g.74285660T>G , CM000666.1:g.74285660T>G	GRCh37
NC_000004.10:g.74504524T>G	NCBI36
NG_009291.1:g.20689T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+304T>G MANE Select	ENSP00000295897.4:n.1785+304T>G
ENST00000295897.8:c.1785+304T>G	ENSP00000295897.4:n.1785+304T>G
ENST00000401494.7:c.1440+304T>G	ENSP00000384695.3:n.1440+304T>G
ENST00000415165.6:c.1209+304T>G	ENSP00000401820.2:n.1209+304T>G
ENST00000476441.6:c.*1064+304T>G	ENSP00000423727.1:n.*1064+304T>G
ENST00000495173.1:n.93+304T>G
ENST00000503124.5:c.1335+304T>G	ENSP00000421027.1:n.1335+304T>G
ENST00000505649.5:n.1332+304T>G
ENST00000508932.5:n.176-311T>G
ENST00000509063.5:c.1785+304T>G	ENSP00000422784.1:n.1785+304T>G
ENST00000511370.1:c.1318+304T>G
ENST00000621085.4:c.1146+304T>G	ENSP00000483421.1:n.1146+304T>G
ENST00000621628.4:c.1146+304T>G	ENSP00000480485.1:n.1146+304T>G
NM_000477.5:c.1785+304T>G	NP_000468.1:n.1785+304T>G
NM_000477.6:c.1785+304T>G	NP_000468.1:n.1785+304T>G
NM_000477.7:c.1785+304T>G MANE Select	NP_000468.1:n.1785+304T>G