Canonical Allele Identifier: CA99701563

Gene: ALB

Linked Data

• dbSNP Id: rs1016981452
• gnomAD v2: 4-74275236-C-A
• gnomAD v3: 4-73409519-C-A
• gnomAD v4: 4-73409519-C-A
• MyVariant Identifiers: chr4:g.74275236C>A (hg19) ; chr4:g.73409519C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409519C>A , CM000666.2:g.73409519C>A	GRCh38
NC_000004.11:g.74275236C>A , CM000666.1:g.74275236C>A	GRCh37
NC_000004.10:g.74494100C>A	NCBI36
NG_009291.1:g.10265C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.615+32C>A MANE Select	ENSP00000295897.4:n.615+32C>A
ENST00000295897.8:c.615+32C>A	ENSP00000295897.4:n.615+32C>A
ENST00000401494.7:c.270+32C>A	ENSP00000384695.3:n.270+32C>A
ENST00000415165.6:c.138-2477C>A	ENSP00000401820.2:n.138-2477C>A
ENST00000476441.6:c.212+32C>A	ENSP00000423727.1:n.212+32C>A
ENST00000503124.5:c.165+32C>A	ENSP00000421027.1:n.165+32C>A
ENST00000505649.5:n.301+32C>A
ENST00000509063.5:c.615+32C>A	ENSP00000422784.1:n.615+32C>A
ENST00000511370.1:c.148+32C>A
ENST00000621085.4:c.490+157C>A	ENSP00000483421.1:n.490+157C>A
ENST00000621628.4:c.486+443C>A	ENSP00000480485.1:n.486+443C>A
NM_000477.5:c.615+32C>A	NP_000468.1:n.615+32C>A
NM_000477.6:c.615+32C>A	NP_000468.1:n.615+32C>A
NM_000477.7:c.615+32C>A MANE Select	NP_000468.1:n.615+32C>A