Canonical Allele Identifier: CA2670966554

Gene: ALB

Linked Data

• gnomAD v4: 4-73419449-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419449T>G , CM000666.2:g.73419449T>G	GRCh38
NC_000004.11:g.74285166T>G , CM000666.1:g.74285166T>G	GRCh37
NC_000004.10:g.74504030T>G	NCBI36
NG_009291.1:g.20195T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1653-58T>G MANE Select	ENSP00000295897.4:n.1653-58T>G
ENST00000295897.8:c.1653-58T>G	ENSP00000295897.4:n.1653-58T>G
ENST00000401494.7:c.1308-58T>G	ENSP00000384695.3:n.1308-58T>G
ENST00000415165.6:c.1077-58T>G	ENSP00000401820.2:n.1077-58T>G
ENST00000476441.6:c.*932-58T>G	ENSP00000423727.1:n.*932-58T>G
ENST00000486939.1:n.307-58T>G
ENST00000503124.5:c.1203-58T>G	ENSP00000421027.1:n.1203-58T>G
ENST00000505649.5:n.1200-58T>G
ENST00000508932.5:n.169T>G
ENST00000509063.5:c.1653-58T>G	ENSP00000422784.1:n.1653-58T>G
ENST00000511370.1:c.1186-58T>G
ENST00000621085.4:c.1014-58T>G	ENSP00000483421.1:n.1014-58T>G
ENST00000621628.4:c.1014-58T>G	ENSP00000480485.1:n.1014-58T>G
NM_000477.5:c.1653-58T>G	NP_000468.1:n.1653-58T>G
NM_000477.6:c.1653-58T>G	NP_000468.1:n.1653-58T>G
NM_000477.7:c.1653-58T>G MANE Select	NP_000468.1:n.1653-58T>G