Canonical Allele Identifier: CA552304212

Gene: ALB

Linked Data

• dbSNP Id: rs1363125037
• gnomAD v2: 4-74270006-A-G
• gnomAD v3: 4-73404289-A-G
• gnomAD v4: 4-73404289-A-G
• MyVariant Identifiers: chr4:g.74270006A>G (hg19) ; chr4:g.73404289A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404289A>G , CM000666.2:g.73404289A>G	GRCh38
NC_000004.11:g.74270006A>G , CM000666.1:g.74270006A>G	GRCh37
NC_000004.10:g.74488870A>G	NCBI36
NG_009291.1:g.5035A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.-39A>G MANE Select	ENSP00000295897.4:n.-39A>G
ENST00000295897.8:c.-39A>G	ENSP00000295897.4:n.-39A>G
ENST00000415165.6:c.-39A>G	ENSP00000401820.2:n.-39A>G
ENST00000441319.5:c.48-80A>G	ENSP00000392541.1:n.48-80A>G
ENST00000510166.5:n.3A>G
ENST00000514786.1:n.1A>G
ENST00000515133.5:n.3A>G
ENST00000621085.4:c.-39A>G	ENSP00000483421.1:n.-39A>G
ENST00000621628.4:c.-39A>G	ENSP00000480485.1:n.-39A>G
NM_000477.5:c.-39A>G	NP_000468.1:n.-39A>G
NM_000477.6:c.-39A>G	NP_000468.1:n.-39A>G
NM_000477.7:c.-39A>G MANE Select	NP_000468.1:n.-39A>G