Canonical Allele Identifier: CA357241148

Gene: ALB

Linked Data

• dbSNP Id: rs776487747
• gnomAD v3: 4-73415070-A-T
• gnomAD v4: 4-73415070-A-T
• MyVariant Identifiers: chr4:g.74280787A>T (hg19) ; chr4:g.73415070A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415070A>T , CM000666.2:g.73415070A>T	GRCh38
NC_000004.11:g.74280787A>T , CM000666.1:g.74280787A>T	GRCh37
NC_000004.10:g.74499651A>T	NCBI36
NG_009291.1:g.15816A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1094A>T MANE Select	ENSP00000295897.4:p.Tyr365Phe
ENST00000295897.8:c.1094A>T	ENSP00000295897.4:p.Tyr365Phe
ENST00000401494.7:c.749A>T	ENSP00000384695.3:p.Tyr250Phe
ENST00000415165.6:c.518A>T	ENSP00000401820.2:p.Tyr173Phe
ENST00000476441.6:c.*373A>T	ENSP00000423727.1:n.*373A>T
ENST00000484992.1:n.414A>T
ENST00000503124.5:c.644A>T	ENSP00000421027.1:p.Tyr215Phe
ENST00000504043.1:n.97A>T
ENST00000505649.5:n.780A>T
ENST00000509063.5:c.1094A>T	ENSP00000422784.1:p.Tyr365Phe
ENST00000511370.1:c.627A>T
ENST00000621085.4:c.491-36A>T	ENSP00000483421.1:n.491-36A>T
ENST00000621628.4:c.487-32A>T	ENSP00000480485.1:n.487-32A>T
NM_000477.5:c.1094A>T	NP_000468.1:p.Tyr365Phe
NM_000477.6:c.1094A>T	NP_000468.1:p.Tyr365Phe
NM_000477.7:c.1094A>T MANE Select	NP_000468.1:p.Tyr365Phe