Canonical Allele Identifier: CA798284593

Gene: ALB

Linked Data

• dbSNP Id: rs1340878638
• gnomAD v3: 4-73406246-G-C
• gnomAD v4: 4-73406246-G-C
• MyVariant Identifiers: chr4:g.74271963G>C (hg19) ; chr4:g.73406246G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406246G>C , CM000666.2:g.73406246G>C	GRCh38
NC_000004.11:g.74271963G>C , CM000666.1:g.74271963G>C	GRCh37
NC_000004.10:g.74490827G>C	NCBI36
NG_009291.1:g.6992G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-383G>C MANE Select	ENSP00000295897.4:n.138-383G>C
ENST00000295897.8:c.138-383G>C	ENSP00000295897.4:n.138-383G>C
ENST00000401494.7:c.137+1073G>C	ENSP00000384695.3:n.137+1073G>C
ENST00000415165.6:c.137+1073G>C	ENSP00000401820.2:n.137+1073G>C
ENST00000441319.5:c.144-383G>C	ENSP00000392541.1:n.144-383G>C
ENST00000476441.6:c.79+1840G>C	ENSP00000423727.1:n.79+1840G>C
ENST00000503124.5:c.-101-383G>C	ENSP00000421027.1:n.-101-383G>C
ENST00000509063.5:c.138-383G>C	ENSP00000422784.1:n.138-383G>C
ENST00000510166.5:n.174-383G>C
ENST00000514786.1:n.107-383G>C
ENST00000515133.5:n.179-383G>C
ENST00000621085.4:c.138-383G>C	ENSP00000483421.1:n.138-383G>C
ENST00000621628.4:c.138-383G>C	ENSP00000480485.1:n.138-383G>C
NM_000477.5:c.138-383G>C	NP_000468.1:n.138-383G>C
NM_000477.6:c.138-383G>C	NP_000468.1:n.138-383G>C
NM_000477.7:c.138-383G>C MANE Select	NP_000468.1:n.138-383G>C