Canonical Allele Identifier: CA357234557

Gene: ALB

Linked Data

• dbSNP Id: rs1577933590
• MyVariant Identifiers: chr4:g.74270082T>C (hg19) ; chr4:g.73404365T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404365T>C , CM000666.2:g.73404365T>C	GRCh38
NC_000004.11:g.74270082T>C , CM000666.1:g.74270082T>C	GRCh37
NC_000004.10:g.74488946T>C	NCBI36
NG_009291.1:g.5111T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.38T>C MANE Select	ENSP00000295897.4:p.Phe13Ser
ENST00000295897.8:c.38T>C	ENSP00000295897.4:p.Phe13Ser
ENST00000401494.7:c.38T>C	ENSP00000384695.3:p.Phe13Ser
ENST00000415165.6:c.38T>C	ENSP00000401820.2:p.Phe13Ser
ENST00000441319.5:c.48-4T>C	ENSP00000392541.1:n.48-4T>C
ENST00000476441.6:c.38T>C	ENSP00000423727.1:p.Phe13Ser
ENST00000503124.5:c.-143T>C	ENSP00000421027.1:n.-143T>C
ENST00000509063.5:c.38T>C	ENSP00000422784.1:p.Phe13Ser
ENST00000510166.5:n.79T>C
ENST00000514786.1:n.48+29T>C
ENST00000515133.5:n.79T>C
ENST00000621085.4:c.38T>C	ENSP00000483421.1:p.Phe13Ser
ENST00000621628.4:c.38T>C	ENSP00000480485.1:p.Phe13Ser
NM_000477.5:c.38T>C	NP_000468.1:p.Phe13Ser
NM_000477.6:c.38T>C	NP_000468.1:p.Phe13Ser
NM_000477.7:c.38T>C MANE Select	NP_000468.1:p.Phe13Ser