Canonical Allele Identifier: CA798289406

Gene: ALB

Linked Data

• dbSNP Id: rs1417099320
• gnomAD v3: 4-73413259-C-G
• gnomAD v4: 4-73413259-C-G
• MyVariant Identifiers: chr4:g.74278976C>G (hg19) ; chr4:g.73413259C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413259C>G , CM000666.2:g.73413259C>G	GRCh38
NC_000004.11:g.74278976C>G , CM000666.1:g.74278976C>G	GRCh37
NC_000004.10:g.74497840C>G	NCBI36
NG_009291.1:g.14005C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.844-161C>G MANE Select	ENSP00000295897.4:n.844-161C>G
ENST00000295897.8:c.844-161C>G	ENSP00000295897.4:n.844-161C>G
ENST00000401494.7:c.499-161C>G	ENSP00000384695.3:n.499-161C>G
ENST00000415165.6:c.268-161C>G	ENSP00000401820.2:n.268-161C>G
ENST00000476441.6:c.*123-161C>G	ENSP00000423727.1:n.*123-161C>G
ENST00000484992.1:n.3C>G
ENST00000503124.5:c.394-161C>G	ENSP00000421027.1:n.394-161C>G
ENST00000505649.5:n.530-161C>G
ENST00000509063.5:c.844-161C>G	ENSP00000422784.1:n.844-161C>G
ENST00000511370.1:c.377-161C>G
ENST00000621085.4:c.491-1847C>G	ENSP00000483421.1:n.491-1847C>G
ENST00000621628.4:c.487-1843C>G	ENSP00000480485.1:n.487-1843C>G
NM_000477.5:c.844-161C>G	NP_000468.1:n.844-161C>G
NM_000477.6:c.844-161C>G	NP_000468.1:n.844-161C>G
NM_000477.7:c.844-161C>G MANE Select	NP_000468.1:n.844-161C>G