Canonical Allele Identifier: CA2959249

Gene: ALB

Linked Data

• dbSNP Id: rs746018746
• ExAC: 4:74270033 G / A
• gnomAD v2: 4-74270033-G-A
• gnomAD v3: 4-73404316-G-A
• gnomAD v4: 4-73404316-G-A
• MyVariant Identifiers: chr4:g.74270033G>A (hg19) ; chr4:g.73404316G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404316G>A , CM000666.2:g.73404316G>A	GRCh38
NC_000004.11:g.74270033G>A , CM000666.1:g.74270033G>A	GRCh37
NC_000004.10:g.74488897G>A	NCBI36
NG_009291.1:g.5062G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.-12G>A MANE Select	ENSP00000295897.4:n.-12G>A
ENST00000295897.8:c.-12G>A	ENSP00000295897.4:n.-12G>A
ENST00000401494.7:c.-12G>A	ENSP00000384695.3:n.-12G>A
ENST00000415165.6:c.-12G>A	ENSP00000401820.2:n.-12G>A
ENST00000441319.5:c.48-53G>A	ENSP00000392541.1:n.48-53G>A
ENST00000476441.6:c.-12G>A	ENSP00000423727.1:n.-12G>A
ENST00000503124.5:c.-192G>A	ENSP00000421027.1:n.-192G>A
ENST00000509063.5:c.-12G>A	ENSP00000422784.1:n.-12G>A
ENST00000510166.5:n.30G>A
ENST00000514786.1:n.28G>A
ENST00000515133.5:n.30G>A
ENST00000621085.4:c.-12G>A	ENSP00000483421.1:n.-12G>A
ENST00000621628.4:c.-12G>A	ENSP00000480485.1:n.-12G>A
NM_000477.5:c.-12G>A	NP_000468.1:n.-12G>A
NM_000477.6:c.-12G>A	NP_000468.1:n.-12G>A
NM_000477.7:c.-12G>A MANE Select	NP_000468.1:n.-12G>A