Canonical Allele Identifier: CA99700927

Gene: ALB

Linked Data

• dbSNP Id: rs1045395244
• gnomAD v3: 4-73409037-A-T
• gnomAD v4: 4-73409037-A-T
• MyVariant Identifiers: chr4:g.74274754A>T (hg19) ; chr4:g.73409037A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409037A>T , CM000666.2:g.73409037A>T	GRCh38
NC_000004.11:g.74274754A>T , CM000666.1:g.74274754A>T	GRCh37
NC_000004.10:g.74493618A>T	NCBI36
NG_009291.1:g.9783A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+232A>T MANE Select	ENSP00000295897.4:n.482+232A>T
ENST00000295897.8:c.482+232A>T	ENSP00000295897.4:n.482+232A>T
ENST00000401494.7:c.138-318A>T	ENSP00000384695.3:n.138-318A>T
ENST00000415165.6:c.138-2959A>T	ENSP00000401820.2:n.138-2959A>T
ENST00000441319.5:c.488+232A>T	ENSP00000392541.1:n.488+232A>T
ENST00000476441.6:c.80-318A>T	ENSP00000423727.1:n.80-318A>T
ENST00000503124.5:c.33-318A>T	ENSP00000421027.1:n.33-318A>T
ENST00000505649.5:n.168+232A>T
ENST00000509063.5:c.482+232A>T	ENSP00000422784.1:n.482+232A>T
ENST00000514786.1:n.451+232A>T
ENST00000621085.4:c.482+232A>T	ENSP00000483421.1:n.482+232A>T
ENST00000621628.4:c.483-36A>T	ENSP00000480485.1:n.483-36A>T
NM_000477.5:c.482+232A>T	NP_000468.1:n.482+232A>T
NM_000477.6:c.482+232A>T	NP_000468.1:n.482+232A>T
NM_000477.7:c.482+232A>T MANE Select	NP_000468.1:n.482+232A>T