Canonical Allele Identifier: CA357245102

Gene: ALB

Linked Data

• dbSNP Id: rs769125333
• gnomAD v2: 4-74283977-A-T
• gnomAD v4: 4-73418260-A-T
• MyVariant Identifiers: chr4:g.74283977A>T (hg19) ; chr4:g.73418260A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418260A>T , CM000666.2:g.73418260A>T	GRCh38
NC_000004.11:g.74283977A>T , CM000666.1:g.74283977A>T	GRCh37
NC_000004.10:g.74502841A>T	NCBI36
NG_009291.1:g.19006A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1601A>T MANE Select	ENSP00000295897.4:p.His534Leu
ENST00000295897.8:c.1601A>T	ENSP00000295897.4:p.His534Leu
ENST00000401494.7:c.1256A>T	ENSP00000384695.3:p.His419Leu
ENST00000415165.6:c.1025A>T	ENSP00000401820.2:p.His342Leu
ENST00000476441.6:c.*880A>T	ENSP00000423727.1:n.*880A>T
ENST00000486939.1:n.255A>T
ENST00000503124.5:c.1151A>T	ENSP00000421027.1:p.His384Leu
ENST00000505649.5:n.1148A>T
ENST00000509063.5:c.1601A>T	ENSP00000422784.1:p.His534Leu
ENST00000511370.1:c.1134A>T
ENST00000621085.4:c.962A>T	ENSP00000483421.1:p.His321Leu
ENST00000621628.4:c.962A>T	ENSP00000480485.1:p.His321Leu
NM_000477.5:c.1601A>T	NP_000468.1:p.His534Leu
NM_000477.6:c.1601A>T	NP_000468.1:p.His534Leu
NM_000477.7:c.1601A>T MANE Select	NP_000468.1:p.His534Leu