Canonical Allele Identifier: CA2600250552

Gene: ALB

Linked Data

• dbSNP Id: rs779014097
• gnomAD v3: 4-73404309-C-T
• gnomAD v4: 4-73404309-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404309C>T , CM000666.2:g.73404309C>T	GRCh38
NC_000004.11:g.74270026C>T , CM000666.1:g.74270026C>T	GRCh37
NC_000004.10:g.74488890C>T	NCBI36
NG_009291.1:g.5055C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.-19C>T MANE Select	ENSP00000295897.4:n.-19C>T
ENST00000295897.8:c.-19C>T	ENSP00000295897.4:n.-19C>T
ENST00000401494.7:c.-19C>T	ENSP00000384695.3:n.-19C>T
ENST00000415165.6:c.-19C>T	ENSP00000401820.2:n.-19C>T
ENST00000441319.5:c.48-60C>T	ENSP00000392541.1:n.48-60C>T
ENST00000476441.6:c.-19C>T	ENSP00000423727.1:n.-19C>T
ENST00000503124.5:c.-199C>T	ENSP00000421027.1:n.-199C>T
ENST00000509063.5:c.-19C>T	ENSP00000422784.1:n.-19C>T
ENST00000510166.5:n.23C>T
ENST00000514786.1:n.21C>T
ENST00000515133.5:n.23C>T
ENST00000621085.4:c.-19C>T	ENSP00000483421.1:n.-19C>T
ENST00000621628.4:c.-19C>T	ENSP00000480485.1:n.-19C>T
NM_000477.5:c.-19C>T	NP_000468.1:n.-19C>T
NM_000477.6:c.-19C>T	NP_000468.1:n.-19C>T
NM_000477.7:c.-19C>T MANE Select	NP_000468.1:n.-19C>T