Canonical Allele Identifier: CA552305371

Gene: ALB

Linked Data

• dbSNP Id: rs1560855647
• gnomAD v2: 4-74275223-G-A
• gnomAD v3: 4-73409506-G-A
• gnomAD v4: 4-73409506-G-A
• MyVariant Identifiers: chr4:g.74275223_74275224delinsAA (hg19) ; chr4:g.73409506_73409507delinsAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409506G>A , CM000666.2:g.73409506G>A	GRCh38
NC_000004.11:g.74275223G>A , CM000666.1:g.74275223G>A	GRCh37
NC_000004.10:g.74494087G>A	NCBI36
NG_009291.1:g.10252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.615+19G>A MANE Select	ENSP00000295897.4:n.615+19G>A
ENST00000295897.8:c.615+19G>A	ENSP00000295897.4:n.615+19G>A
ENST00000401494.7:c.270+19G>A	ENSP00000384695.3:n.270+19G>A
ENST00000415165.6:c.138-2490G>A	ENSP00000401820.2:n.138-2490G>A
ENST00000476441.6:c.212+19G>A	ENSP00000423727.1:n.212+19G>A
ENST00000503124.5:c.165+19G>A	ENSP00000421027.1:n.165+19G>A
ENST00000505649.5:n.301+19G>A
ENST00000509063.5:c.615+19G>A	ENSP00000422784.1:n.615+19G>A
ENST00000511370.1:c.148+19G>A
ENST00000621085.4:c.490+144G>A	ENSP00000483421.1:n.490+144G>A
ENST00000621628.4:c.486+430G>A	ENSP00000480485.1:n.486+430G>A
NM_000477.5:c.615+19G>A	NP_000468.1:n.615+19G>A
NM_000477.6:c.615+19G>A	NP_000468.1:n.615+19G>A
NM_000477.7:c.615+19G>A MANE Select	NP_000468.1:n.615+19G>A