Canonical Allele Identifier: CA99710533

Gene: ALB

Linked Data

• dbSNP Id: rs17853250
• gnomAD v3: 4-73418249-A-G
• gnomAD v4: 4-73418249-A-G
• MyVariant Identifiers: chr4:g.74283966A>G (hg19) ; chr4:g.73418249A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418249A>G , CM000666.2:g.73418249A>G	GRCh38
NC_000004.11:g.74283966A>G , CM000666.1:g.74283966A>G	GRCh37
NC_000004.10:g.74502830A>G	NCBI36
NG_009291.1:g.18995A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1590A>G MANE Select	ENSP00000295897.4:p.Thr530=
ENST00000295897.8:c.1590A>G	ENSP00000295897.4:p.Thr530=
ENST00000401494.7:c.1245A>G	ENSP00000384695.3:p.Thr415=
ENST00000415165.6:c.1014A>G	ENSP00000401820.2:p.Thr338=
ENST00000476441.6:c.*869A>G	ENSP00000423727.1:n.*869A>G
ENST00000486939.1:n.244A>G
ENST00000503124.5:c.1140A>G	ENSP00000421027.1:p.Thr380=
ENST00000505649.5:n.1137A>G
ENST00000509063.5:c.1590A>G	ENSP00000422784.1:p.Thr530=
ENST00000511370.1:c.1123A>G
ENST00000621085.4:c.951A>G	ENSP00000483421.1:p.Thr317=
ENST00000621628.4:c.951A>G	ENSP00000480485.1:p.Thr317=
NM_000477.5:c.1590A>G	NP_000468.1:p.Thr530=
NM_000477.6:c.1590A>G	NP_000468.1:p.Thr530=
NM_000477.7:c.1590A>G MANE Select	NP_000468.1:p.Thr530=