Canonical Allele Identifier: CA2959675

Gene: ALB

Linked Data

• dbSNP Id: rs776185501
• ExAC: 4:74283848 C / A
• gnomAD v2: 4-74283848-C-A
• gnomAD v3: 4-73418131-C-A
• gnomAD v4: 4-73418131-C-A
• MyVariant Identifiers: chr4:g.74283848C>A (hg19) ; chr4:g.73418131C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418131C>A , CM000666.2:g.73418131C>A	GRCh38
NC_000004.11:g.74283848C>A , CM000666.1:g.74283848C>A	GRCh37
NC_000004.10:g.74502712C>A	NCBI36
NG_009291.1:g.18877C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1472C>A MANE Select	ENSP00000295897.4:p.Thr491Lys
ENST00000295897.8:c.1472C>A	ENSP00000295897.4:p.Thr491Lys
ENST00000401494.7:c.1127C>A	ENSP00000384695.3:p.Thr376Lys
ENST00000415165.6:c.896C>A	ENSP00000401820.2:p.Thr299Lys
ENST00000476441.6:c.*751C>A	ENSP00000423727.1:n.*751C>A
ENST00000486939.1:n.126C>A
ENST00000503124.5:c.1022C>A	ENSP00000421027.1:p.Thr341Lys
ENST00000505649.5:n.1019C>A
ENST00000509063.5:c.1472C>A	ENSP00000422784.1:p.Thr491Lys
ENST00000511370.1:c.1005C>A
ENST00000621085.4:c.833C>A	ENSP00000483421.1:p.Thr278Lys
ENST00000621628.4:c.833C>A	ENSP00000480485.1:p.Thr278Lys
NM_000477.5:c.1472C>A	NP_000468.1:p.Thr491Lys
NM_000477.6:c.1472C>A	NP_000468.1:p.Thr491Lys
NM_000477.7:c.1472C>A MANE Select	NP_000468.1:p.Thr491Lys