Canonical Allele Identifier: CA2670937293

Gene: ALB

Linked Data

• gnomAD v4: 4-73409257-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409257T>A , CM000666.2:g.73409257T>A	GRCh38
NC_000004.11:g.74274974T>A , CM000666.1:g.74274974T>A	GRCh37
NC_000004.10:g.74493838T>A	NCBI36
NG_009291.1:g.10003T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-98T>A MANE Select	ENSP00000295897.4:n.483-98T>A
ENST00000295897.8:c.483-98T>A	ENSP00000295897.4:n.483-98T>A
ENST00000401494.7:c.138-98T>A	ENSP00000384695.3:n.138-98T>A
ENST00000415165.6:c.138-2739T>A	ENSP00000401820.2:n.138-2739T>A
ENST00000441319.5:c.489-98T>A	ENSP00000392541.1:n.489-98T>A
ENST00000476441.6:c.80-98T>A	ENSP00000423727.1:n.80-98T>A
ENST00000503124.5:c.33-98T>A	ENSP00000421027.1:n.33-98T>A
ENST00000505649.5:n.169-98T>A
ENST00000509063.5:c.483-98T>A	ENSP00000422784.1:n.483-98T>A
ENST00000514786.1:n.452-98T>A
ENST00000621085.4:c.483-98T>A	ENSP00000483421.1:n.483-98T>A
ENST00000621628.4:c.486+181T>A	ENSP00000480485.1:n.486+181T>A
NM_000477.5:c.483-98T>A	NP_000468.1:n.483-98T>A
NM_000477.6:c.483-98T>A	NP_000468.1:n.483-98T>A
NM_000477.7:c.483-98T>A MANE Select	NP_000468.1:n.483-98T>A