Canonical Allele Identifier: CA439948415

Gene: ALB

Linked Data

• dbSNP Id: rs745553711
• MyVariant Identifiers: chr4:g.74283975C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418258C>T , CM000666.2:g.73418258C>T	GRCh38
NC_000004.11:g.74283975C>T , CM000666.1:g.74283975C>T	GRCh37
NC_000004.10:g.74502839C>T	NCBI36
NG_009291.1:g.19004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1599C>T MANE Select	ENSP00000295897.4:p.Phe533=
ENST00000295897.8:c.1599C>T	ENSP00000295897.4:p.Phe533=
ENST00000401494.7:c.1254C>T	ENSP00000384695.3:p.Phe418=
ENST00000415165.6:c.1023C>T	ENSP00000401820.2:p.Phe341=
ENST00000476441.6:c.*878C>T	ENSP00000423727.1:n.*878C>T
ENST00000486939.1:n.253C>T
ENST00000503124.5:c.1149C>T	ENSP00000421027.1:p.Phe383=
ENST00000505649.5:n.1146C>T
ENST00000509063.5:c.1599C>T	ENSP00000422784.1:p.Phe533=
ENST00000511370.1:c.1132C>T
ENST00000621085.4:c.960C>T	ENSP00000483421.1:p.Phe320=
ENST00000621628.4:c.960C>T	ENSP00000480485.1:p.Phe320=
NM_000477.5:c.1599C>T	NP_000468.1:p.Phe533=
NM_000477.6:c.1599C>T	NP_000468.1:p.Phe533=
NM_000477.7:c.1599C>T MANE Select	NP_000468.1:p.Phe533=