Canonical Allele Identifier: CA2670936466

Gene: ALB

Linked Data

• gnomAD v4: 4-73404325-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404325A>G , CM000666.2:g.73404325A>G	GRCh38
NC_000004.11:g.74270042A>G , CM000666.1:g.74270042A>G	GRCh37
NC_000004.10:g.74488906A>G	NCBI36
NG_009291.1:g.5071A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.-3A>G MANE Select	ENSP00000295897.4:n.-3A>G
ENST00000295897.8:c.-3A>G	ENSP00000295897.4:n.-3A>G
ENST00000401494.7:c.-3A>G	ENSP00000384695.3:n.-3A>G
ENST00000415165.6:c.-3A>G	ENSP00000401820.2:n.-3A>G
ENST00000441319.5:c.48-44A>G	ENSP00000392541.1:n.48-44A>G
ENST00000476441.6:c.-3A>G	ENSP00000423727.1:n.-3A>G
ENST00000503124.5:c.-183A>G	ENSP00000421027.1:n.-183A>G
ENST00000509063.5:c.-3A>G	ENSP00000422784.1:n.-3A>G
ENST00000510166.5:n.39A>G
ENST00000514786.1:n.37A>G
ENST00000515133.5:n.39A>G
ENST00000621085.4:c.-3A>G	ENSP00000483421.1:n.-3A>G
ENST00000621628.4:c.-3A>G	ENSP00000480485.1:n.-3A>G
NM_000477.5:c.-3A>G	NP_000468.1:n.-3A>G
NM_000477.6:c.-3A>G	NP_000468.1:n.-3A>G
NM_000477.7:c.-3A>G MANE Select	NP_000468.1:n.-3A>G