Canonical Allele Identifier: CA99696280

Gene: ALB

Linked Data

• dbSNP Id: rs759533235
• gnomAD v2: 4-74269981-G-A
• gnomAD v3: 4-73404264-G-A
• gnomAD v4: 4-73404264-G-A
• MyVariant Identifiers: chr4:g.74269981G>A (hg19) ; chr4:g.73404264G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404264G>A , CM000666.2:g.73404264G>A	GRCh38
NC_000004.11:g.74269981G>A , CM000666.1:g.74269981G>A	GRCh37
NC_000004.10:g.74488845G>A	NCBI36
NG_009291.1:g.5010G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.8:c.-64G>A	ENSP00000295897.4:n.-64G>A
ENST00000441319.5:c.48-105G>A	ENSP00000392541.1:n.48-105G>A
ENST00000621628.4:c.-64G>A	ENSP00000480485.1:n.-64G>A
NM_000477.5:c.-64G>A	NP_000468.1:n.-64G>A
NM_000477.6:c.-64G>A	NP_000468.1:n.-64G>A